Name: rs57592028
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs57592028

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:14615805-14615833 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₆ / del(T)₁₅ / del(T)₁₄ / d…
del(T)₁₆ / del(T)₁₅ / del(T)₁₄ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉ / dup(T)₂₀ / dup(T)₂₂ / ins(T)₃₁ / ins(T)₃₂ / ins(T)₃₃ / ins(T)₃₄ / ins(T)₄₀ / ins(T)₄₈
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.0689 (481/6981, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC107984996 : Non Coding Transcript Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6981	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8665	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0613, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0689, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0033, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.878749	0.019026	0.102225	32
European	Sub	6537	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8574	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0655, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0736, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0035, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.869399	0.020493	0.110108	32
African	Sub	140	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	136	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	28	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	160	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	88	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6981	(T)₂₉=0.8665	del(T)₁₆=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0613, delTT=0.0689, delT=0.0000, dupT=0.0033, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6537	(T)₂₉=0.8574	del(T)₁₆=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0655, delTT=0.0736, delT=0.0000, dupT=0.0035, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	160	(T)₂₉=1.000	del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	African	Sub	140	(T)₂₉=1.000	del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	88	(T)₂₉=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	28	(T)₂₉=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(T)₂₉=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₂₉=1.0	del(T)₁₆=0.0, del(T)₁₅=0.0, del(T)₁₄=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 17	NC_000017.11:g.14615818_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615819_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615820_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615822_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615823_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615824_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615825_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615826_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615827_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615828_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615829_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615830_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615831_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615832_14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615833del
GRCh38.p14 chr 17	NC_000017.11:g.14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615832_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615831_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615830_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615829_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615828_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615827_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615826_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615825_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615824_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615823_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615822_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615821_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615820_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615819_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615818_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615817_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615816_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615815_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615814_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615812_14615833dup
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519135_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519136_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519137_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519139_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519140_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519141_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519142_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519143_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519144_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519145_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519146_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519147_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519148_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519149_14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519150del
GRCh37.p13 chr 17	NC_000017.10:g.14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519149_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519148_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519147_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519146_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519145_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519144_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519143_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519142_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519141_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519140_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519139_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519138_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519137_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519136_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519135_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519134_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519133_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519132_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519131_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519129_14519150dup
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LOC107984996, uncharacterized LOC107984996 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107984996 transcript	XR_001753052.2:n.	N/A	Non Coding Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₉=	del(T)₁₆	del(T)₁₅	del(T)₁₄	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉	dup(T)₂₀	dup(T)₂₂	ins(T)₃₁	ins(T)₃₂	ins(T)₃₃	ins(T)₃₄	ins(T)₄₀	ins(T)₄₈
GRCh38.p14 chr 17	NC_000017.11:g.14615805_14615833=	NC_000017.11:g.14615818_14615833del	NC_000017.11:g.14615819_14615833del	NC_000017.11:g.14615820_14615833del	NC_000017.11:g.14615822_14615833del	NC_000017.11:g.14615823_14615833del	NC_000017.11:g.14615824_14615833del	NC_000017.11:g.14615825_14615833del	NC_000017.11:g.14615826_14615833del	NC_000017.11:g.14615827_14615833del	NC_000017.11:g.14615828_14615833del	NC_000017.11:g.14615829_14615833del	NC_000017.11:g.14615830_14615833del	NC_000017.11:g.14615831_14615833del	NC_000017.11:g.14615832_14615833del	NC_000017.11:g.14615833del	NC_000017.11:g.14615833dup	NC_000017.11:g.14615832_14615833dup	NC_000017.11:g.14615831_14615833dup	NC_000017.11:g.14615830_14615833dup	NC_000017.11:g.14615829_14615833dup	NC_000017.11:g.14615828_14615833dup	NC_000017.11:g.14615827_14615833dup	NC_000017.11:g.14615826_14615833dup	NC_000017.11:g.14615825_14615833dup	NC_000017.11:g.14615824_14615833dup	NC_000017.11:g.14615823_14615833dup	NC_000017.11:g.14615822_14615833dup	NC_000017.11:g.14615821_14615833dup	NC_000017.11:g.14615820_14615833dup	NC_000017.11:g.14615819_14615833dup	NC_000017.11:g.14615818_14615833dup	NC_000017.11:g.14615817_14615833dup	NC_000017.11:g.14615816_14615833dup	NC_000017.11:g.14615815_14615833dup	NC_000017.11:g.14615814_14615833dup	NC_000017.11:g.14615812_14615833dup	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.14615833_14615834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.14519122_14519150=	NC_000017.10:g.14519135_14519150del	NC_000017.10:g.14519136_14519150del	NC_000017.10:g.14519137_14519150del	NC_000017.10:g.14519139_14519150del	NC_000017.10:g.14519140_14519150del	NC_000017.10:g.14519141_14519150del	NC_000017.10:g.14519142_14519150del	NC_000017.10:g.14519143_14519150del	NC_000017.10:g.14519144_14519150del	NC_000017.10:g.14519145_14519150del	NC_000017.10:g.14519146_14519150del	NC_000017.10:g.14519147_14519150del	NC_000017.10:g.14519148_14519150del	NC_000017.10:g.14519149_14519150del	NC_000017.10:g.14519150del	NC_000017.10:g.14519150dup	NC_000017.10:g.14519149_14519150dup	NC_000017.10:g.14519148_14519150dup	NC_000017.10:g.14519147_14519150dup	NC_000017.10:g.14519146_14519150dup	NC_000017.10:g.14519145_14519150dup	NC_000017.10:g.14519144_14519150dup	NC_000017.10:g.14519143_14519150dup	NC_000017.10:g.14519142_14519150dup	NC_000017.10:g.14519141_14519150dup	NC_000017.10:g.14519140_14519150dup	NC_000017.10:g.14519139_14519150dup	NC_000017.10:g.14519138_14519150dup	NC_000017.10:g.14519137_14519150dup	NC_000017.10:g.14519136_14519150dup	NC_000017.10:g.14519135_14519150dup	NC_000017.10:g.14519134_14519150dup	NC_000017.10:g.14519133_14519150dup	NC_000017.10:g.14519132_14519150dup	NC_000017.10:g.14519131_14519150dup	NC_000017.10:g.14519129_14519150dup	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.14519150_14519151insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

76 SubSNP, 55 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80068234	Dec 14, 2007 (129)
2	HGSV	ss80425329	Dec 14, 2007 (129)
3	HGSV	ss83694013	Dec 14, 2007 (129)
4	HUMANGENOME_JCVI	ss95689793	Mar 15, 2016 (147)
5	HUMANGENOME_JCVI	ss96565614	Mar 15, 2016 (147)
6	GMI	ss289317853	May 04, 2012 (137)
7	PJP	ss294906299	May 09, 2011 (134)
8	SSMP	ss664344303	Apr 01, 2015 (144)
9	SWEGEN	ss3015246612	Nov 08, 2017 (151)
10	MCHAISSO	ss3063861567	Jan 10, 2018 (151)
11	MCHAISSO	ss3065641648	Jan 10, 2018 (151)
12	EVA_DECODE	ss3700148152	Jul 13, 2019 (153)
13	EVA_DECODE	ss3700148153	Jul 13, 2019 (153)
14	EVA_DECODE	ss3700148155	Jul 13, 2019 (153)
15	EVA_DECODE	ss3700148156	Jul 13, 2019 (153)
16	ACPOP	ss3741901173	Jul 13, 2019 (153)
17	ACPOP	ss3741901174	Jul 13, 2019 (153)
18	ACPOP	ss3741901175	Jul 13, 2019 (153)
19	EVA	ss3834797481	Apr 27, 2020 (154)
20	KOGIC	ss3978463948	Apr 27, 2020 (154)
21	KOGIC	ss3978463949	Apr 27, 2020 (154)
22	KOGIC	ss3978463950	Apr 27, 2020 (154)
23	KOGIC	ss3978463951	Apr 27, 2020 (154)
24	KOGIC	ss3978463952	Apr 27, 2020 (154)
25	GNOMAD	ss4308437101	Apr 26, 2021 (155)
26	GNOMAD	ss4308437102	Apr 26, 2021 (155)
27	GNOMAD	ss4308437121	Apr 26, 2021 (155)
28	GNOMAD	ss4308437122	Apr 26, 2021 (155)
29	GNOMAD	ss4308437123	Apr 26, 2021 (155)
30	GNOMAD	ss4308437124	Apr 26, 2021 (155)
31	GNOMAD	ss4308437125	Apr 26, 2021 (155)
32	GNOMAD	ss4308437126	Apr 26, 2021 (155)
33	GNOMAD	ss4308437127	Apr 26, 2021 (155)
34	GNOMAD	ss4308437128	Apr 26, 2021 (155)
35	GNOMAD	ss4308437129	Apr 26, 2021 (155)
36	GNOMAD	ss4308437130	Apr 26, 2021 (155)
37	GNOMAD	ss4308437131	Apr 26, 2021 (155)
38	GNOMAD	ss4308437132	Apr 26, 2021 (155)
39	GNOMAD	ss4308437133	Apr 26, 2021 (155)
40	GNOMAD	ss4308437134	Apr 26, 2021 (155)
41	GNOMAD	ss4308437135	Apr 26, 2021 (155)
42	GNOMAD	ss4308437136	Apr 26, 2021 (155)
43	GNOMAD	ss4308437137	Apr 26, 2021 (155)
44	GNOMAD	ss4308437138	Apr 26, 2021 (155)
45	GNOMAD	ss4308437139	Apr 26, 2021 (155)
46	GNOMAD	ss4308437140	Apr 26, 2021 (155)
47	GNOMAD	ss4308437141	Apr 26, 2021 (155)
48	GNOMAD	ss4308437142	Apr 26, 2021 (155)
49	GNOMAD	ss4308437143	Apr 26, 2021 (155)
50	GNOMAD	ss4308437144	Apr 26, 2021 (155)
51	GNOMAD	ss4308437145	Apr 26, 2021 (155)
52	GNOMAD	ss4308437146	Apr 26, 2021 (155)
53	GNOMAD	ss4308437147	Apr 26, 2021 (155)
54	GNOMAD	ss4308437148	Apr 26, 2021 (155)
55	GNOMAD	ss4308437149	Apr 26, 2021 (155)
56	GNOMAD	ss4308437150	Apr 26, 2021 (155)
57	GNOMAD	ss4308437151	Apr 26, 2021 (155)
58	GNOMAD	ss4308437152	Apr 26, 2021 (155)
59	GNOMAD	ss4308437153	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5221633520	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5221633521	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5221633522	Apr 26, 2021 (155)
63	TOMMO_GENOMICS	ss5221633523	Apr 26, 2021 (155)
64	TOMMO_GENOMICS	ss5221633524	Apr 26, 2021 (155)
65	1000G_HIGH_COVERAGE	ss5302534861	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5495700664	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5495700665	Oct 16, 2022 (156)
68	HUGCELL_USP	ss5495700666	Oct 16, 2022 (156)
69	HUGCELL_USP	ss5495700667	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5777268383	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5777268384	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5777268385	Oct 16, 2022 (156)
73	TOMMO_GENOMICS	ss5777268386	Oct 16, 2022 (156)
74	TOMMO_GENOMICS	ss5777268387	Oct 16, 2022 (156)
75	TOMMO_GENOMICS	ss5777268388	Oct 16, 2022 (156)
76	EVA	ss5851754970	Oct 16, 2022 (156)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502297399 (NC_000017.11:14615804::T 683/88196) Row 502297400 (NC_000017.11:14615804::TT 19/88308) Row 502297419 (NC_000017.11:14615804::TTT 6/88310)...	-	Apr 26, 2021 (155)
112	Korean Genome Project Submission ignored due to conflicting rows: Row 34841949 (NC_000017.11:14615806:TTT: 251/1760) Row 34841950 (NC_000017.11:14615807:TT: 556/1760) Row 34841951 (NC_000017.11:14615808:T: 34/1760)...	-	Apr 27, 2020 (154)
113	Korean Genome Project Submission ignored due to conflicting rows: Row 34841949 (NC_000017.11:14615806:TTT: 251/1760) Row 34841950 (NC_000017.11:14615807:TT: 556/1760) Row 34841951 (NC_000017.11:14615808:T: 34/1760)...	-	Apr 27, 2020 (154)
114	Korean Genome Project Submission ignored due to conflicting rows: Row 34841949 (NC_000017.11:14615806:TTT: 251/1760) Row 34841950 (NC_000017.11:14615807:TT: 556/1760) Row 34841951 (NC_000017.11:14615808:T: 34/1760)...	-	Apr 27, 2020 (154)
115	Korean Genome Project Submission ignored due to conflicting rows: Row 34841949 (NC_000017.11:14615806:TTT: 251/1760) Row 34841950 (NC_000017.11:14615807:TT: 556/1760) Row 34841951 (NC_000017.11:14615808:T: 34/1760)...	-	Apr 27, 2020 (154)
116	Korean Genome Project Submission ignored due to conflicting rows: Row 34841949 (NC_000017.11:14615806:TTT: 251/1760) Row 34841950 (NC_000017.11:14615807:TT: 556/1760) Row 34841951 (NC_000017.11:14615808:T: 34/1760)...	-	Apr 27, 2020 (154)
117	Northern Sweden Submission ignored due to conflicting rows: Row 15186038 (NC_000017.10:14519121:TT: 57/554) Row 15186039 (NC_000017.10:14519121::TTTTTTTTTTTTTT 8/554) Row 15186040 (NC_000017.10:14519121::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/554)	-	Jul 13, 2019 (153)
118	Northern Sweden Submission ignored due to conflicting rows: Row 15186038 (NC_000017.10:14519121:TT: 57/554) Row 15186039 (NC_000017.10:14519121::TTTTTTTTTTTTTT 8/554) Row 15186040 (NC_000017.10:14519121::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/554)	-	Jul 13, 2019 (153)
119	Northern Sweden Submission ignored due to conflicting rows: Row 15186038 (NC_000017.10:14519121:TT: 57/554) Row 15186039 (NC_000017.10:14519121::TTTTTTTTTTTTTT 8/554) Row 15186040 (NC_000017.10:14519121::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/554)	-	Jul 13, 2019 (153)
120	8.3KJPN Submission ignored due to conflicting rows: Row 79602827 (NC_000017.10:14519121:TT: 4703/16498) Row 79602828 (NC_000017.10:14519121:TTT: 2334/16498) Row 79602829 (NC_000017.10:14519121:TTTT: 66/16498)...	-	Apr 26, 2021 (155)
121	8.3KJPN Submission ignored due to conflicting rows: Row 79602827 (NC_000017.10:14519121:TT: 4703/16498) Row 79602828 (NC_000017.10:14519121:TTT: 2334/16498) Row 79602829 (NC_000017.10:14519121:TTTT: 66/16498)...	-	Apr 26, 2021 (155)
122	8.3KJPN Submission ignored due to conflicting rows: Row 79602827 (NC_000017.10:14519121:TT: 4703/16498) Row 79602828 (NC_000017.10:14519121:TTT: 2334/16498) Row 79602829 (NC_000017.10:14519121:TTTT: 66/16498)...	-	Apr 26, 2021 (155)
123	8.3KJPN Submission ignored due to conflicting rows: Row 79602827 (NC_000017.10:14519121:TT: 4703/16498) Row 79602828 (NC_000017.10:14519121:TTT: 2334/16498) Row 79602829 (NC_000017.10:14519121:TTTT: 66/16498)...	-	Apr 26, 2021 (155)
124	8.3KJPN Submission ignored due to conflicting rows: Row 79602827 (NC_000017.10:14519121:TT: 4703/16498) Row 79602828 (NC_000017.10:14519121:TTT: 2334/16498) Row 79602829 (NC_000017.10:14519121:TTTT: 66/16498)...	-	Apr 26, 2021 (155)
125	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
126	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
127	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
128	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
129	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
130	14KJPN Submission ignored due to conflicting rows: Row 111105487 (NC_000017.11:14615804:TT: 8242/25054) Row 111105488 (NC_000017.11:14615804:TTTT: 122/25054) Row 111105489 (NC_000017.11:14615804:TTT: 4070/25054)...	-	Oct 16, 2022 (156)
131	ALFA	NC_000017.11 - 14615805	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs199820922	May 11, 2012 (137)
rs71352494	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4308437153	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4308437152	NC_000017.11:14615804:TTTTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4308437151	NC_000017.11:14615804:TTTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437150	NC_000017.11:14615804:TTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3978463952, ss4308437149	NC_000017.11:14615804:TTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5221633522	NC_000017.10:14519121:TTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3700148152, ss4308437148, ss5495700666, ss5777268384	NC_000017.11:14615804:TTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3978463951	NC_000017.11:14615805:TTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3015246612, ss5221633521	NC_000017.10:14519121:TTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437147, ss5302534861, ss5495700665, ss5777268385	NC_000017.11:14615804:TTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3700148153	NC_000017.11:14615805:TTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3978463948	NC_000017.11:14615806:TTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss289317853	NC_000017.9:14459846:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80068234, ss80425329, ss83694013, ss294906299	NC_000017.9:14459873:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss664344303, ss3741901173, ss3834797481, ss5221633520	NC_000017.10:14519121:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3063861567, ss3065641648, ss4308437146, ss5495700664, ss5777268383, ss5851754970	NC_000017.11:14615804:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3700148155	NC_000017.11:14615806:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3978463949	NC_000017.11:14615807:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss96565614	NT_010718.16:14122499:TT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5221633523	NC_000017.10:14519121:T:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437145, ss5495700667, ss5777268387	NC_000017.11:14615804:T:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3978463950	NC_000017.11:14615808:T:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss96565614	NT_010718.16:14122499:TT:T	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95689793	NT_010718.16:14122523:T:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5221633524	NC_000017.10:14519121::T	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437101, ss5777268386	NC_000017.11:14615804::T	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3700148156	NC_000017.11:14615808::T	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437102, ss5777268388	NC_000017.11:14615804::TT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11713673555	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95689793	NT_010718.16:14122523:T:TTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437121	NC_000017.11:14615804::TTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437122	NC_000017.11:14615804::TTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437123	NC_000017.11:14615804::TTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437124	NC_000017.11:14615804::TTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437125	NC_000017.11:14615804::TTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437126	NC_000017.11:14615804::TTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437127	NC_000017.11:14615804::TTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437128	NC_000017.11:14615804::TTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437129	NC_000017.11:14615804::TTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437130	NC_000017.11:14615804::TTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437131	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741901174	NC_000017.10:14519121::TTTTTTTTTTT… NC_000017.10:14519121::TTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437132	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437133	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437134	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437135	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437136	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437137	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437138	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437139	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437140	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437141	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437142	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437143	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741901175	NC_000017.10:14519121::TTTTTTTTTTT… NC_000017.10:14519121::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4308437144	NC_000017.11:14615804::TTTTTTTTTTT… NC_000017.11:14615804::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3258016890	NC_000017.11:14615804:TTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
ss3258016891	NC_000017.11:14615804:TTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss3258016894	NC_000017.11:14615804:TTTTTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
ss3258016895	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTT:	NC_000017.11:14615804:TTTTTTTTTTTT… NC_000017.11:14615804:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs57592028

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs57592028