Name: rs753013686
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.

rs753013686

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:89824711-89824732 (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(A)₁₃ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₃ / del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₉ / dup(A)₁₂ / dup(A)₁₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₀=0.000004 (1/264690, TOPMED)
del(A)₁₃=0.0000 (0/5296, ALFA)
del(A)₁₀=0.0000 (0/5296, ALFA) (+ 13 more)
del(A)₈=0.0000 (0/5296, ALFA)
del(A)₇=0.0000 (0/5296, ALFA)
del(A)₆=0.0000 (0/5296, ALFA)
del(A)₅=0.0000 (0/5296, ALFA)
del(A)₄=0.0000 (0/5296, ALFA)
delAAA=0.0000 (0/5296, ALFA)
delAA=0.0000 (0/5296, ALFA)
delA=0.0000 (0/5296, ALFA)
dupA=0.0000 (0/5296, ALFA)
dupAA=0.0000 (0/5296, ALFA)
dupAAA=0.0000 (0/5296, ALFA)
dup(A)₄=0.0000 (0/5296, ALFA)
dupAA=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	HWEP
Total	Global	5296	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3216	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1296	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	44	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1252	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	92	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	76	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	74	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	364	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	40	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	214	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₂=0.999996	del(A)₁₀=0.000004
Allele Frequency Aggregator	Total	Global	5296	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	3216	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	1296	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	364	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	214	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	92	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	74	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	40	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupAA=0.38

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 6	NC_000006.12:g.89824720_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824722_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824723_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824725_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824726_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824727_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824728_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824729_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824730_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824731_89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824732del
GRCh38.p14 chr 6	NC_000006.12:g.89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824731_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824730_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824729_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824728_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824727_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824724_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824721_89824732dup
GRCh38.p14 chr 6	NC_000006.12:g.89824717_89824732dup
GRCh37.p13 chr 6	NC_000006.11:g.90534439_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534441_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534442_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534444_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534445_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534446_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534447_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534448_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534449_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534450_90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534451del
GRCh37.p13 chr 6	NC_000006.11:g.90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534450_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534449_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534448_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534447_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534446_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534443_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534440_90534451dup
GRCh37.p13 chr 6	NC_000006.11:g.90534436_90534451dup
MDN1 RefSeqGene	NG_034012.1:g.72_84del
MDN1 RefSeqGene	NG_034012.1:g.74_84del
MDN1 RefSeqGene	NG_034012.1:g.75_84del
MDN1 RefSeqGene	NG_034012.1:g.77_84del
MDN1 RefSeqGene	NG_034012.1:g.78_84del
MDN1 RefSeqGene	NG_034012.1:g.79_84del
MDN1 RefSeqGene	NG_034012.1:g.80_84del
MDN1 RefSeqGene	NG_034012.1:g.81_84del
MDN1 RefSeqGene	NG_034012.1:g.82_84del
MDN1 RefSeqGene	NG_034012.1:g.83_84del
MDN1 RefSeqGene	NG_034012.1:g.84del
MDN1 RefSeqGene	NG_034012.1:g.84dup
MDN1 RefSeqGene	NG_034012.1:g.83_84dup
MDN1 RefSeqGene	NG_034012.1:g.82_84dup
MDN1 RefSeqGene	NG_034012.1:g.81_84dup
MDN1 RefSeqGene	NG_034012.1:g.80_84dup
MDN1 RefSeqGene	NG_034012.1:g.79_84dup
MDN1 RefSeqGene	NG_034012.1:g.76_84dup
MDN1 RefSeqGene	NG_034012.1:g.73_84dup
MDN1 RefSeqGene	NG_034012.1:g.69_84dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20065_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20067_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20068_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20070_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20071_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20072_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20073_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20074_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20075_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20076_20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20077del
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20076_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20075_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20074_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20073_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20072_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20069_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20066_20077dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20062_20077dup

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	(A)₂₂=	del(A)₁₃	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₉	dup(A)₁₂	dup(A)₁₆
GRCh38.p14 chr 6	NC_000006.12:g.89824711_89824732=	NC_000006.12:g.89824720_89824732del	NC_000006.12:g.89824722_89824732del	NC_000006.12:g.89824723_89824732del	NC_000006.12:g.89824725_89824732del	NC_000006.12:g.89824726_89824732del	NC_000006.12:g.89824727_89824732del	NC_000006.12:g.89824728_89824732del	NC_000006.12:g.89824729_89824732del	NC_000006.12:g.89824730_89824732del	NC_000006.12:g.89824731_89824732del	NC_000006.12:g.89824732del	NC_000006.12:g.89824732dup	NC_000006.12:g.89824731_89824732dup	NC_000006.12:g.89824730_89824732dup	NC_000006.12:g.89824729_89824732dup	NC_000006.12:g.89824728_89824732dup	NC_000006.12:g.89824727_89824732dup	NC_000006.12:g.89824724_89824732dup	NC_000006.12:g.89824721_89824732dup	NC_000006.12:g.89824717_89824732dup
GRCh37.p13 chr 6	NC_000006.11:g.90534430_90534451=	NC_000006.11:g.90534439_90534451del	NC_000006.11:g.90534441_90534451del	NC_000006.11:g.90534442_90534451del	NC_000006.11:g.90534444_90534451del	NC_000006.11:g.90534445_90534451del	NC_000006.11:g.90534446_90534451del	NC_000006.11:g.90534447_90534451del	NC_000006.11:g.90534448_90534451del	NC_000006.11:g.90534449_90534451del	NC_000006.11:g.90534450_90534451del	NC_000006.11:g.90534451del	NC_000006.11:g.90534451dup	NC_000006.11:g.90534450_90534451dup	NC_000006.11:g.90534449_90534451dup	NC_000006.11:g.90534448_90534451dup	NC_000006.11:g.90534447_90534451dup	NC_000006.11:g.90534446_90534451dup	NC_000006.11:g.90534443_90534451dup	NC_000006.11:g.90534440_90534451dup	NC_000006.11:g.90534436_90534451dup
MDN1 RefSeqGene	NG_034012.1:g.63_84=	NG_034012.1:g.72_84del	NG_034012.1:g.74_84del	NG_034012.1:g.75_84del	NG_034012.1:g.77_84del	NG_034012.1:g.78_84del	NG_034012.1:g.79_84del	NG_034012.1:g.80_84del	NG_034012.1:g.81_84del	NG_034012.1:g.82_84del	NG_034012.1:g.83_84del	NG_034012.1:g.84del	NG_034012.1:g.84dup	NG_034012.1:g.83_84dup	NG_034012.1:g.82_84dup	NG_034012.1:g.81_84dup	NG_034012.1:g.80_84dup	NG_034012.1:g.79_84dup	NG_034012.1:g.76_84dup	NG_034012.1:g.73_84dup	NG_034012.1:g.69_84dup
GRCh38.p14 chr 6 fix patch HG2121_PATCH	NW_017363815.1:g.20056_20077=	NW_017363815.1:g.20065_20077del	NW_017363815.1:g.20067_20077del	NW_017363815.1:g.20068_20077del	NW_017363815.1:g.20070_20077del	NW_017363815.1:g.20071_20077del	NW_017363815.1:g.20072_20077del	NW_017363815.1:g.20073_20077del	NW_017363815.1:g.20074_20077del	NW_017363815.1:g.20075_20077del	NW_017363815.1:g.20076_20077del	NW_017363815.1:g.20077del	NW_017363815.1:g.20077dup	NW_017363815.1:g.20076_20077dup	NW_017363815.1:g.20075_20077dup	NW_017363815.1:g.20074_20077dup	NW_017363815.1:g.20073_20077dup	NW_017363815.1:g.20072_20077dup	NW_017363815.1:g.20069_20077dup	NW_017363815.1:g.20066_20077dup	NW_017363815.1:g.20062_20077dup

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#.

35 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_GENOME_DK	ss1576807837	Apr 01, 2015 (144)
2	EVA	ss3830063952	Apr 26, 2020 (154)
3	KOGIC	ss3959564161	Apr 26, 2020 (154)
4	KOGIC	ss3959564162	Apr 26, 2020 (154)
5	KOGIC	ss3959564163	Apr 26, 2020 (154)
6	KOGIC	ss3959564164	Apr 26, 2020 (154)
7	GNOMAD	ss4146562745	Apr 26, 2021 (155)
8	GNOMAD	ss4146562746	Apr 26, 2021 (155)
9	GNOMAD	ss4146562747	Apr 26, 2021 (155)
10	GNOMAD	ss4146562748	Apr 26, 2021 (155)
11	GNOMAD	ss4146562749	Apr 26, 2021 (155)
12	GNOMAD	ss4146562750	Apr 26, 2021 (155)
13	GNOMAD	ss4146562751	Apr 26, 2021 (155)
14	GNOMAD	ss4146562752	Apr 26, 2021 (155)
15	GNOMAD	ss4146562753	Apr 26, 2021 (155)
16	GNOMAD	ss4146562755	Apr 26, 2021 (155)
17	GNOMAD	ss4146562756	Apr 26, 2021 (155)
18	GNOMAD	ss4146562757	Apr 26, 2021 (155)
19	GNOMAD	ss4146562758	Apr 26, 2021 (155)
20	GNOMAD	ss4146562759	Apr 26, 2021 (155)
21	GNOMAD	ss4146562760	Apr 26, 2021 (155)
22	GNOMAD	ss4146562761	Apr 26, 2021 (155)
23	GNOMAD	ss4146562762	Apr 26, 2021 (155)
24	GNOMAD	ss4146562763	Apr 26, 2021 (155)
25	TOPMED	ss4712409058	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5178724733	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5178724734	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5269407985	Oct 14, 2022 (156)
29	HUGCELL_USP	ss5466941722	Oct 14, 2022 (156)
30	HUGCELL_USP	ss5466941723	Oct 14, 2022 (156)
31	HUGCELL_USP	ss5466941724	Oct 14, 2022 (156)
32	HUGCELL_USP	ss5466941726	Oct 14, 2022 (156)
33	TOMMO_GENOMICS	ss5717256466	Oct 14, 2022 (156)
34	TOMMO_GENOMICS	ss5717256468	Oct 14, 2022 (156)
35	TOMMO_GENOMICS	ss5717256469	Oct 14, 2022 (156)
36	The Danish reference pan genome	NC_000006.11 - 90534430	Apr 26, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 233167007 (NC_000006.12:89824710::A 21346/59154) Row 233167008 (NC_000006.12:89824710::AA 230/58612) Row 233167009 (NC_000006.12:89824710::AAA 92/58950)...	-	Apr 26, 2021 (155)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 15942162 (NC_000006.12:89824712::A 192/1708) Row 15942163 (NC_000006.12:89824711:A: 184/1708) Row 15942164 (NC_000006.12:89824712::AA 46/1708)...	-	Apr 26, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 15942162 (NC_000006.12:89824712::A 192/1708) Row 15942163 (NC_000006.12:89824711:A: 184/1708) Row 15942164 (NC_000006.12:89824712::AA 46/1708)...	-	Apr 26, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 15942162 (NC_000006.12:89824712::A 192/1708) Row 15942163 (NC_000006.12:89824711:A: 184/1708) Row 15942164 (NC_000006.12:89824712::AA 46/1708)...	-	Apr 26, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 15942162 (NC_000006.12:89824712::A 192/1708) Row 15942163 (NC_000006.12:89824711:A: 184/1708) Row 15942164 (NC_000006.12:89824712::AA 46/1708)...	-	Apr 26, 2020 (154)
59	8.3KJPN Submission ignored due to conflicting rows: Row 36694040 (NC_000006.11:90534429::A 457/16726) Row 36694041 (NC_000006.11:90534429:A: 31/16726)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 36694040 (NC_000006.11:90534429::A 457/16726) Row 36694041 (NC_000006.11:90534429:A: 31/16726)	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 51093570 (NC_000006.12:89824710::A 848/28216) Row 51093572 (NC_000006.12:89824710:A: 50/28216) Row 51093573 (NC_000006.12:89824710:AAAAAAAAAAA: 2/28216)	-	Oct 14, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 51093570 (NC_000006.12:89824710::A 848/28216) Row 51093572 (NC_000006.12:89824710:A: 50/28216) Row 51093573 (NC_000006.12:89824710:AAAAAAAAAAA: 2/28216)	-	Oct 14, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 51093570 (NC_000006.12:89824710::A 848/28216) Row 51093572 (NC_000006.12:89824710:A: 50/28216) Row 51093573 (NC_000006.12:89824710:AAAAAAAAAAA: 2/28216)	-	Oct 14, 2022 (156)
64	TopMed	NC_000006.12 - 89824711	Apr 26, 2021 (155)
65	ALFA	NC_000006.12 - 89824711	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4146562763	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss5717256469	NC_000006.12:89824710:AAAAAAAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA
549786616, ss4146562762, ss4712409058	NC_000006.12:89824710:AAAAAAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4146562761	NC_000006.12:89824710:AAAAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4146562760	NC_000006.12:89824710:AAAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4146562759	NC_000006.12:89824710:AAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4146562758	NC_000006.12:89824710:AAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4146562757	NC_000006.12:89824710:AAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3959564164, ss4146562756, ss5466941726	NC_000006.12:89824710:AA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5178724734	NC_000006.11:90534429:A:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562755, ss5269407985, ss5466941724, ss5717256468	NC_000006.12:89824710:A:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3959564162	NC_000006.12:89824711:A:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3830063952, ss5178724733	NC_000006.11:90534429::A	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562745, ss5466941722, ss5717256466	NC_000006.12:89824710::A	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3959564161	NC_000006.12:89824712::A	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
1091679, ss1576807837	NC_000006.11:90534429::AA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562746, ss5466941723	NC_000006.12:89824710::AA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3959564163	NC_000006.12:89824712::AA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562747	NC_000006.12:89824710::AAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562748	NC_000006.12:89824710::AAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4054304568	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562749	NC_000006.12:89824710::AAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562750	NC_000006.12:89824710::AAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562751	NC_000006.12:89824710::AAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562752	NC_000006.12:89824710::AAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4146562753	NC_000006.12:89824710::AAAAAAAAAAA… NC_000006.12:89824710::AAAAAAAAAAAAAAAA	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3504756770	NC_000006.12:89824710:AAAAAA:	NC_000006.12:89824710:AAAAAAAAAAAA… NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

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

No publications for rs753013686

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs753013686