Name: rs71034774
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.

rs71034774

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:10562947-10562971 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / 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)₁₂ / dup(T)₁₄ / dup(T)₁₅ / ins(T)₂₉ / ins(T)₃₅ / ins(T)₃₇
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.000057 (15/264690, TOPMED)
dupT=0.1452 (1107/7624, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IRAG1-AS1 : Intron Variant
LYVE1 : Intron 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	7624	TTTTTTTTTTTTTTTTTTTTTTTTT=0.8286	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0043, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1452, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0114, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0088, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017	0.818865	0.102115	0.079021	32
European	Sub	6408	TTTTTTTTTTTTTTTTTTTTTTTTT=0.7965	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0051, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1726, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0133, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0105, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020	0.782129	0.122825	0.095047	32
African	Sub	906	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	44	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	862	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	48	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	102	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	120	TTTTTTTTTTTTTTTTTTTTTTTTT=0.975	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.008, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.017, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	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
TopMed	Global	Study-wide	264690	(T)₂₅=0.999943	del(T)₁₀=0.000057
Allele Frequency Aggregator	Total	Global	7624	(T)₂₅=0.8286	del(T)₁₄=0.0000, del(T)₁₃=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=0.0043, delTT=0.0000, delT=0.0000, dupT=0.1452, dupTT=0.0114, dupTTT=0.0088, dup(T)₄=0.0017
Allele Frequency Aggregator	European	Sub	6408	(T)₂₅=0.7965	del(T)₁₄=0.0000, del(T)₁₃=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=0.0051, delTT=0.0000, delT=0.0000, dupT=0.1726, dupTT=0.0133, dupTTT=0.0105, dup(T)₄=0.0020
Allele Frequency Aggregator	African	Sub	906	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=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, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	120	(T)₂₅=0.975	del(T)₁₄=0.000, del(T)₁₃=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=0.008, dupTT=0.017, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	102	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=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, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	48	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=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, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=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, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	18	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=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, dupTTT=0.00, dup(T)₄=0.00

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 11	NC_000011.10:g.10562958_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562959_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562960_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562961_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562962_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562963_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562964_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562965_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562966_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562967_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562968_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562969_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562970_10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562971del
GRCh38.p14 chr 11	NC_000011.10:g.10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562970_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562969_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562968_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562967_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562966_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562965_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562964_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562963_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562962_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562960_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562958_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562957_10562971dup
GRCh38.p14 chr 11	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 11	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 11	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.10584505_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584506_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584507_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584508_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584509_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584510_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584511_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584512_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584513_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584514_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584515_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584516_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584517_10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584518del
GRCh37.p13 chr 11	NC_000011.9:g.10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584517_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584516_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584515_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584514_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584513_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584512_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584511_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584510_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584509_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584507_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584505_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584504_10584518dup
GRCh37.p13 chr 11	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LYVE1, lymphatic vessel endothelial hyaluronan receptor 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LYVE1 transcript	NM_006691.4:c.397+980_397… NM_006691.4:c.397+980_397+993del	N/A	Intron Variant

Gene: IRAG1-AS1, IRAG1 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IRAG1-AS1 transcript variant 3	NR_034093.2:n.	N/A	Intron Variant
IRAG1-AS1 transcript variant 4	NR_034094.2:n.	N/A	Intron Variant
IRAG1-AS1 transcript variant 1	NR_046374.1:n.	N/A	Intron Variant
IRAG1-AS1 transcript variant 2	NR_046375.1:n.	N/A	Intron 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)₂₅=	del(T)₁₄	del(T)₁₃	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)₁₂	dup(T)₁₄	dup(T)₁₅	ins(T)₂₉	ins(T)₃₅	ins(T)₃₇
GRCh38.p14 chr 11	NC_000011.10:g.10562947_10562971=	NC_000011.10:g.10562958_10562971del	NC_000011.10:g.10562959_10562971del	NC_000011.10:g.10562960_10562971del	NC_000011.10:g.10562961_10562971del	NC_000011.10:g.10562962_10562971del	NC_000011.10:g.10562963_10562971del	NC_000011.10:g.10562964_10562971del	NC_000011.10:g.10562965_10562971del	NC_000011.10:g.10562966_10562971del	NC_000011.10:g.10562967_10562971del	NC_000011.10:g.10562968_10562971del	NC_000011.10:g.10562969_10562971del	NC_000011.10:g.10562970_10562971del	NC_000011.10:g.10562971del	NC_000011.10:g.10562971dup	NC_000011.10:g.10562970_10562971dup	NC_000011.10:g.10562969_10562971dup	NC_000011.10:g.10562968_10562971dup	NC_000011.10:g.10562967_10562971dup	NC_000011.10:g.10562966_10562971dup	NC_000011.10:g.10562965_10562971dup	NC_000011.10:g.10562964_10562971dup	NC_000011.10:g.10562963_10562971dup	NC_000011.10:g.10562962_10562971dup	NC_000011.10:g.10562960_10562971dup	NC_000011.10:g.10562958_10562971dup	NC_000011.10:g.10562957_10562971dup	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:g.10562971_10562972insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.10584494_10584518=	NC_000011.9:g.10584505_10584518del	NC_000011.9:g.10584506_10584518del	NC_000011.9:g.10584507_10584518del	NC_000011.9:g.10584508_10584518del	NC_000011.9:g.10584509_10584518del	NC_000011.9:g.10584510_10584518del	NC_000011.9:g.10584511_10584518del	NC_000011.9:g.10584512_10584518del	NC_000011.9:g.10584513_10584518del	NC_000011.9:g.10584514_10584518del	NC_000011.9:g.10584515_10584518del	NC_000011.9:g.10584516_10584518del	NC_000011.9:g.10584517_10584518del	NC_000011.9:g.10584518del	NC_000011.9:g.10584518dup	NC_000011.9:g.10584517_10584518dup	NC_000011.9:g.10584516_10584518dup	NC_000011.9:g.10584515_10584518dup	NC_000011.9:g.10584514_10584518dup	NC_000011.9:g.10584513_10584518dup	NC_000011.9:g.10584512_10584518dup	NC_000011.9:g.10584511_10584518dup	NC_000011.9:g.10584510_10584518dup	NC_000011.9:g.10584509_10584518dup	NC_000011.9:g.10584507_10584518dup	NC_000011.9:g.10584505_10584518dup	NC_000011.9:g.10584504_10584518dup	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.9:g.10584518_10584519insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
LYVE1 transcript	NM_006691.3:c.397+993=	NM_006691.3:c.397+980_397+993del	NM_006691.3:c.397+981_397+993del	NM_006691.3:c.397+982_397+993del	NM_006691.3:c.397+983_397+993del	NM_006691.3:c.397+984_397+993del	NM_006691.3:c.397+985_397+993del	NM_006691.3:c.397+986_397+993del	NM_006691.3:c.397+987_397+993del	NM_006691.3:c.397+988_397+993del	NM_006691.3:c.397+989_397+993del	NM_006691.3:c.397+990_397+993del	NM_006691.3:c.397+991_397+993del	NM_006691.3:c.397+992_397+993del	NM_006691.3:c.397+993del	NM_006691.3:c.397+993dup	NM_006691.3:c.397+992_397+993dup	NM_006691.3:c.397+991_397+993dup	NM_006691.3:c.397+990_397+993dup	NM_006691.3:c.397+989_397+993dup	NM_006691.3:c.397+988_397+993dup	NM_006691.3:c.397+987_397+993dup	NM_006691.3:c.397+986_397+993dup	NM_006691.3:c.397+985_397+993dup	NM_006691.3:c.397+984_397+993dup	NM_006691.3:c.397+982_397+993dup	NM_006691.3:c.397+980_397+993dup	NM_006691.3:c.397+979_397+993dup	NM_006691.3:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_006691.3:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_006691.3:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
LYVE1 transcript	NM_006691.4:c.397+993=	NM_006691.4:c.397+980_397+993del	NM_006691.4:c.397+981_397+993del	NM_006691.4:c.397+982_397+993del	NM_006691.4:c.397+983_397+993del	NM_006691.4:c.397+984_397+993del	NM_006691.4:c.397+985_397+993del	NM_006691.4:c.397+986_397+993del	NM_006691.4:c.397+987_397+993del	NM_006691.4:c.397+988_397+993del	NM_006691.4:c.397+989_397+993del	NM_006691.4:c.397+990_397+993del	NM_006691.4:c.397+991_397+993del	NM_006691.4:c.397+992_397+993del	NM_006691.4:c.397+993del	NM_006691.4:c.397+993dup	NM_006691.4:c.397+992_397+993dup	NM_006691.4:c.397+991_397+993dup	NM_006691.4:c.397+990_397+993dup	NM_006691.4:c.397+989_397+993dup	NM_006691.4:c.397+988_397+993dup	NM_006691.4:c.397+987_397+993dup	NM_006691.4:c.397+986_397+993dup	NM_006691.4:c.397+985_397+993dup	NM_006691.4:c.397+984_397+993dup	NM_006691.4:c.397+982_397+993dup	NM_006691.4:c.397+980_397+993dup	NM_006691.4:c.397+979_397+993dup	NM_006691.4:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_006691.4:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_006691.4:c.397+993_397+994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
LYVE1 transcript variant X1	XM_005252759.1:c.86-2147=	XM_005252759.1:c.86-2160_86-2147del	XM_005252759.1:c.86-2159_86-2147del	XM_005252759.1:c.86-2158_86-2147del	XM_005252759.1:c.86-2157_86-2147del	XM_005252759.1:c.86-2156_86-2147del	XM_005252759.1:c.86-2155_86-2147del	XM_005252759.1:c.86-2154_86-2147del	XM_005252759.1:c.86-2153_86-2147del	XM_005252759.1:c.86-2152_86-2147del	XM_005252759.1:c.86-2151_86-2147del	XM_005252759.1:c.86-2150_86-2147del	XM_005252759.1:c.86-2149_86-2147del	XM_005252759.1:c.86-2148_86-2147del	XM_005252759.1:c.86-2147del	XM_005252759.1:c.86-2147dup	XM_005252759.1:c.86-2148_86-2147dup	XM_005252759.1:c.86-2149_86-2147dup	XM_005252759.1:c.86-2150_86-2147dup	XM_005252759.1:c.86-2151_86-2147dup	XM_005252759.1:c.86-2152_86-2147dup	XM_005252759.1:c.86-2153_86-2147dup	XM_005252759.1:c.86-2154_86-2147dup	XM_005252759.1:c.86-2155_86-2147dup	XM_005252759.1:c.86-2156_86-2147dup	XM_005252759.1:c.86-2158_86-2147dup	XM_005252759.1:c.86-2160_86-2147dup	XM_005252759.1:c.86-2161_86-2147dup	XM_005252759.1:c.86-2147_86-2146insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252759.1:c.86-2147_86-2146insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005252759.1:c.86-2147_86-2146insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

54 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95560326	Feb 13, 2009 (130)
2	GMI	ss287869991	Mar 15, 2016 (147)
3	PJP	ss294688725	May 09, 2011 (137)
4	SWEGEN	ss3007594120	Nov 08, 2017 (151)
5	EVA	ss3832476964	Apr 26, 2020 (154)
6	GNOMAD	ss4229981078	Apr 26, 2021 (155)
7	GNOMAD	ss4229981079	Apr 26, 2021 (155)
8	GNOMAD	ss4229981080	Apr 26, 2021 (155)
9	GNOMAD	ss4229981081	Apr 26, 2021 (155)
10	GNOMAD	ss4229981082	Apr 26, 2021 (155)
11	GNOMAD	ss4229981083	Apr 26, 2021 (155)
12	GNOMAD	ss4229981084	Apr 26, 2021 (155)
13	GNOMAD	ss4229981085	Apr 26, 2021 (155)
14	GNOMAD	ss4229981086	Apr 26, 2021 (155)
15	GNOMAD	ss4229981087	Apr 26, 2021 (155)
16	GNOMAD	ss4229981088	Apr 26, 2021 (155)
17	GNOMAD	ss4229981089	Apr 26, 2021 (155)
18	GNOMAD	ss4229981090	Apr 26, 2021 (155)
19	GNOMAD	ss4229981091	Apr 26, 2021 (155)
20	GNOMAD	ss4229981093	Apr 26, 2021 (155)
21	GNOMAD	ss4229981094	Apr 26, 2021 (155)
22	GNOMAD	ss4229981095	Apr 26, 2021 (155)
23	GNOMAD	ss4229981096	Apr 26, 2021 (155)
24	GNOMAD	ss4229981097	Apr 26, 2021 (155)
25	GNOMAD	ss4229981098	Apr 26, 2021 (155)
26	GNOMAD	ss4229981099	Apr 26, 2021 (155)
27	GNOMAD	ss4229981100	Apr 26, 2021 (155)
28	GNOMAD	ss4229981101	Apr 26, 2021 (155)
29	GNOMAD	ss4229981102	Apr 26, 2021 (155)
30	GNOMAD	ss4229981103	Apr 26, 2021 (155)
31	GNOMAD	ss4229981104	Apr 26, 2021 (155)
32	GNOMAD	ss4229981105	Apr 26, 2021 (155)
33	TOPMED	ss4875073840	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5200671990	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5200671991	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5200671992	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5200671993	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5200671994	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5286393701	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5286393702	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5286393703	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5286393704	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5481696806	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5481696808	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5481696809	Oct 16, 2022 (156)
46	SANFORD_IMAGENETICS	ss5650631248	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5747423005	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5747423007	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5747423008	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5747423009	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5747423010	Oct 16, 2022 (156)
52	EVA	ss5836258963	Oct 16, 2022 (156)
53	EVA	ss5836258964	Oct 16, 2022 (156)
54	EVA	ss5836258965	Oct 16, 2022 (156)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 371264327 (NC_000011.10:10562946::TTT 2359/75752) Row 371264328 (NC_000011.10:10562946::TTTT 332/75700) Row 371264329 (NC_000011.10:10562946::TTTTT 126/75688)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 58641297 (NC_000011.9:10584493::T 5780/15988) Row 58641298 (NC_000011.9:10584493::TTT 228/15988) Row 58641299 (NC_000011.9:10584493::TT 328/15988)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 58641297 (NC_000011.9:10584493::T 5780/15988) Row 58641298 (NC_000011.9:10584493::TTT 228/15988) Row 58641299 (NC_000011.9:10584493::TT 328/15988)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 58641297 (NC_000011.9:10584493::T 5780/15988) Row 58641298 (NC_000011.9:10584493::TTT 228/15988) Row 58641299 (NC_000011.9:10584493::TT 328/15988)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 58641297 (NC_000011.9:10584493::T 5780/15988) Row 58641298 (NC_000011.9:10584493::TTT 228/15988) Row 58641299 (NC_000011.9:10584493::TT 328/15988)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 58641297 (NC_000011.9:10584493::T 5780/15988) Row 58641298 (NC_000011.9:10584493::TTT 228/15988) Row 58641299 (NC_000011.9:10584493::TT 328/15988)...	-	Apr 26, 2021 (155)
87	14KJPN Submission ignored due to conflicting rows: Row 81260109 (NC_000011.10:10562946::T 11778/27496) Row 81260111 (NC_000011.10:10562946::TTT 404/27496) Row 81260112 (NC_000011.10:10562946:TTTTTT: 450/27496)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 81260109 (NC_000011.10:10562946::T 11778/27496) Row 81260111 (NC_000011.10:10562946::TTT 404/27496) Row 81260112 (NC_000011.10:10562946:TTTTTT: 450/27496)...	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 81260109 (NC_000011.10:10562946::T 11778/27496) Row 81260111 (NC_000011.10:10562946::TTT 404/27496) Row 81260112 (NC_000011.10:10562946:TTTTTT: 450/27496)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 81260109 (NC_000011.10:10562946::T 11778/27496) Row 81260111 (NC_000011.10:10562946::TTT 404/27496) Row 81260112 (NC_000011.10:10562946:TTTTTT: 450/27496)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 81260109 (NC_000011.10:10562946::T 11778/27496) Row 81260111 (NC_000011.10:10562946::TTT 404/27496) Row 81260112 (NC_000011.10:10562946:TTTTTT: 450/27496)...	-	Oct 16, 2022 (156)
92	TopMed	NC_000011.10 - 10562947	Apr 26, 2021 (155)
93	ALFA	NC_000011.10 - 10562947	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)
rs142976756	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4229981105	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5650631248	NC_000011.9:10584493:TTTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss4229981104	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3007594120	NC_000011.9:10584493:TTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4229981103	NC_000011.10:10562946:TTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss287869991	NT_009237.18:10524493:TTTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4229981102	NC_000011.10:10562946:TTTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
90619496, ss4229981101, ss4875073840	NC_000011.10:10562946:TTTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4229981100	NC_000011.10:10562946:TTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4229981099	NC_000011.10:10562946:TTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5200671993	NC_000011.9:10584493:TTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4229981098, ss5747423008	NC_000011.10:10562946:TTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4229981097	NC_000011.10:10562946:TTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4229981096	NC_000011.10:10562946:TTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981095, ss5286393702, ss5481696809	NC_000011.10:10562946:TTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981094	NC_000011.10:10562946:TT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981093, ss5286393704, ss5481696808	NC_000011.10:10562946:T:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294688725	NC_000011.8:10541070::T	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3832476964, ss5200671990	NC_000011.9:10584493::T	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5481696806, ss5747423005	NC_000011.10:10562946::T	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95560326	NT_009237.18:10524518::T	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5200671992, ss5836258965	NC_000011.9:10584493::TT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5286393701, ss5747423009	NC_000011.10:10562946::TT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5200671991, ss5836258963	NC_000011.9:10584493::TTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981078, ss5286393703, ss5747423007	NC_000011.10:10562946::TTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5200671994, ss5836258964	NC_000011.9:10584493::TTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981079, ss5747423010	NC_000011.10:10562946::TTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11064068990	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981080	NC_000011.10:10562946::TTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981081	NC_000011.10:10562946::TTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981082	NC_000011.10:10562946::TTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981083	NC_000011.10:10562946::TTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981084	NC_000011.10:10562946::TTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981085	NC_000011.10:10562946::TTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981086	NC_000011.10:10562946::TTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981087	NC_000011.10:10562946::TTTTTTTTTTT… NC_000011.10:10562946::TTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981088	NC_000011.10:10562946::TTTTTTTTTTT… NC_000011.10:10562946::TTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981089	NC_000011.10:10562946::TTTTTTTTTTT… NC_000011.10:10562946::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981090	NC_000011.10:10562946::TTTTTTTTTTT… NC_000011.10:10562946::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229981091	NC_000011.10:10562946::TTTTTTTTTTT… NC_000011.10:10562946::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3136989203	NC_000011.10:10562946:TTTTTTTTT:	NC_000011.10:10562946:TTTTTTTTTTTT… NC_000011.10:10562946:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

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

No publications for rs71034774

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

rs71034774