Name: rs35998206
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.

rs35998206

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:26525637-26525657 (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)₉ / del(A)₈ / del(A)₇ / del(…
del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.02494 (346/13872, ALFA)
dupA=0.061 (36/592, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HCG11 : Non Coding Transcript Variant
LOC107986583 : 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	13872	AAAAAAAAAAAAAAAAAAAAA=0.97448	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00058, AAAAAAAAAAAAAAAAAAAAAA=0.02494, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.956006	0.006078	0.037916	32
European	Sub	10657	AAAAAAAAAAAAAAAAAAAAA=0.96678	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00075, AAAAAAAAAAAAAAAAAAAAAA=0.03247, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.942674	0.00792	0.049406	32
African	Sub	1974	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	74	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1900	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	78	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	122	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	546	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	399	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13872	(A)₂₁=0.97448	del(A)₉=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00058, dupA=0.02494, dupAA=0.00000, dupAAA=0.00000
Allele Frequency Aggregator	European	Sub	10657	(A)₂₁=0.96678	del(A)₉=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00075, dupA=0.03247, dupAA=0.00000, dupAAA=0.00000
Allele Frequency Aggregator	African	Sub	1974	(A)₂₁=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=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
Allele Frequency Aggregator	Latin American 2	Sub	546	(A)₂₁=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₇=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
Allele Frequency Aggregator	Other	Sub	399	(A)₂₁=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₇=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
Allele Frequency Aggregator	Latin American 1	Sub	122	(A)₂₁=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₇=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
Allele Frequency Aggregator	Asian	Sub	94	(A)₂₁=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₇=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
Allele Frequency Aggregator	South Asian	Sub	80	(A)₂₁=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₇=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
Northern Sweden	ACPOP	Study-wide	592	- No frequency provided	dupA=0.061

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.26525649_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525650_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525651_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525652_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525654_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525655_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525656_26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525657del
GRCh38.p14 chr 6	NC_000006.12:g.26525657dup
GRCh38.p14 chr 6	NC_000006.12:g.26525656_26525657dup
GRCh38.p14 chr 6	NC_000006.12:g.26525655_26525657dup
GRCh38.p14 chr 6	NC_000006.12:g.26525654_26525657dup
GRCh37.p13 chr 6	NC_000006.11:g.26525877_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525878_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525879_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525880_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525882_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525883_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525884_26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525885del
GRCh37.p13 chr 6	NC_000006.11:g.26525885dup
GRCh37.p13 chr 6	NC_000006.11:g.26525884_26525885dup
GRCh37.p13 chr 6	NC_000006.11:g.26525883_26525885dup
GRCh37.p13 chr 6	NC_000006.11:g.26525882_26525885dup
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71829_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71830_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71831_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71832_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71834_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71835_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71836_71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71837del
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71837dup
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71836_71837dup
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71835_71837dup
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71834_71837dup

Gene: HCG11, HLA complex group 11 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HCG11 transcript	NR_026790.1:n.3944_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3945_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3946_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3947_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3949_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3950_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3951_3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3952del	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3952dup	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3951_3952dup	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3950_3952dup	N/A	Non Coding Transcript Variant
HCG11 transcript	NR_026790.1:n.3949_3952dup	N/A	Non Coding Transcript Variant

Gene: LOC107986583, uncharacterized LOC107986583 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107986583 transcript	XR_001744057.3:n.1754_176… XR_001744057.3:n.1754_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1755_176… XR_001744057.3:n.1755_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1756_176… XR_001744057.3:n.1756_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1757_176… XR_001744057.3:n.1757_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1759_176… XR_001744057.3:n.1759_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1760_176… XR_001744057.3:n.1760_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1761_176… XR_001744057.3:n.1761_1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1762del	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1762dup	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1761_176… XR_001744057.3:n.1761_1762dup	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1760_176… XR_001744057.3:n.1760_1762dup	N/A	Non Coding Transcript Variant
LOC107986583 transcript	XR_001744057.3:n.1759_176… XR_001744057.3:n.1759_1762dup	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	(A)₂₁=	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 6	NC_000006.12:g.26525637_26525657=	NC_000006.12:g.26525649_26525657del	NC_000006.12:g.26525650_26525657del	NC_000006.12:g.26525651_26525657del	NC_000006.12:g.26525652_26525657del	NC_000006.12:g.26525654_26525657del	NC_000006.12:g.26525655_26525657del	NC_000006.12:g.26525656_26525657del	NC_000006.12:g.26525657del	NC_000006.12:g.26525657dup	NC_000006.12:g.26525656_26525657dup	NC_000006.12:g.26525655_26525657dup	NC_000006.12:g.26525654_26525657dup
GRCh37.p13 chr 6	NC_000006.11:g.26525865_26525885=	NC_000006.11:g.26525877_26525885del	NC_000006.11:g.26525878_26525885del	NC_000006.11:g.26525879_26525885del	NC_000006.11:g.26525880_26525885del	NC_000006.11:g.26525882_26525885del	NC_000006.11:g.26525883_26525885del	NC_000006.11:g.26525884_26525885del	NC_000006.11:g.26525885del	NC_000006.11:g.26525885dup	NC_000006.11:g.26525884_26525885dup	NC_000006.11:g.26525883_26525885dup	NC_000006.11:g.26525882_26525885dup
GRCh38.p14 chr 6 novel patch HSCHR6_1_CTG1	NW_025791780.1:g.71817_71837=	NW_025791780.1:g.71829_71837del	NW_025791780.1:g.71830_71837del	NW_025791780.1:g.71831_71837del	NW_025791780.1:g.71832_71837del	NW_025791780.1:g.71834_71837del	NW_025791780.1:g.71835_71837del	NW_025791780.1:g.71836_71837del	NW_025791780.1:g.71837del	NW_025791780.1:g.71837dup	NW_025791780.1:g.71836_71837dup	NW_025791780.1:g.71835_71837dup	NW_025791780.1:g.71834_71837dup
LOC107986583 transcript	XR_001744057.3:n.1742_1762=	XR_001744057.3:n.1754_1762del	XR_001744057.3:n.1755_1762del	XR_001744057.3:n.1756_1762del	XR_001744057.3:n.1757_1762del	XR_001744057.3:n.1759_1762del	XR_001744057.3:n.1760_1762del	XR_001744057.3:n.1761_1762del	XR_001744057.3:n.1762del	XR_001744057.3:n.1762dup	XR_001744057.3:n.1761_1762dup	XR_001744057.3:n.1760_1762dup	XR_001744057.3:n.1759_1762dup
HCG11 transcript	NR_026790.1:n.3932_3952=	NR_026790.1:n.3944_3952del	NR_026790.1:n.3945_3952del	NR_026790.1:n.3946_3952del	NR_026790.1:n.3947_3952del	NR_026790.1:n.3949_3952del	NR_026790.1:n.3950_3952del	NR_026790.1:n.3951_3952del	NR_026790.1:n.3952del	NR_026790.1:n.3952dup	NR_026790.1:n.3951_3952dup	NR_026790.1:n.3950_3952dup	NR_026790.1:n.3949_3952dup
LOC107986583 transcript	XR_007069486.1:n.1742_1762=	XR_007069486.1:n.1754_1762del	XR_007069486.1:n.1755_1762del	XR_007069486.1:n.1756_1762del	XR_007069486.1:n.1757_1762del	XR_007069486.1:n.1759_1762del	XR_007069486.1:n.1760_1762del	XR_007069486.1:n.1761_1762del	XR_007069486.1:n.1762del	XR_007069486.1:n.1762dup	XR_007069486.1:n.1761_1762dup	XR_007069486.1:n.1760_1762dup	XR_007069486.1:n.1759_1762dup

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#.

47 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42718527	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95950587	Dec 05, 2013 (138)
3	PJP	ss295271117	May 09, 2011 (137)
4	SWEGEN	ss2998706589	Nov 17, 2017 (151)
5	MCHAISSO	ss3065074355	Nov 08, 2017 (151)
6	ACPOP	ss3733309171	Jul 13, 2019 (153)
7	PACBIO	ss3785406237	Jul 13, 2019 (153)
8	PACBIO	ss3790767103	Jul 13, 2019 (153)
9	PACBIO	ss3795644446	Jul 13, 2019 (153)
10	EVA	ss3829797416	Apr 26, 2020 (154)
11	KOGIC	ss3958726147	Apr 26, 2020 (154)
12	KOGIC	ss3958726148	Apr 26, 2020 (154)
13	KOGIC	ss3958726149	Apr 26, 2020 (154)
14	KOGIC	ss3958726150	Apr 26, 2020 (154)
15	KOGIC	ss3958726151	Apr 26, 2020 (154)
16	FSA-LAB	ss3984331954	Apr 26, 2021 (155)
17	EVA	ss3986033769	Apr 26, 2021 (155)
18	GNOMAD	ss4138802166	Apr 26, 2021 (155)
19	GNOMAD	ss4138802167	Apr 26, 2021 (155)
20	GNOMAD	ss4138802168	Apr 26, 2021 (155)
21	GNOMAD	ss4138802169	Apr 26, 2021 (155)
22	GNOMAD	ss4138802170	Apr 26, 2021 (155)
23	GNOMAD	ss4138802171	Apr 26, 2021 (155)
24	GNOMAD	ss4138802172	Apr 26, 2021 (155)
25	GNOMAD	ss4138802173	Apr 26, 2021 (155)
26	GNOMAD	ss4138802174	Apr 26, 2021 (155)
27	TOPMED	ss4697344093	Apr 26, 2021 (155)
28	TOPMED	ss4697344094	Apr 26, 2021 (155)
29	TOPMED	ss4697344095	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5176661333	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5176661334	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5176661335	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5176661336	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5176661337	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5267801383	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5267801385	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5267801386	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5267801387	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5465558911	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5465558913	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5465558914	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5465558915	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5714469478	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5714469479	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5714469480	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5714469481	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5714469483	Oct 13, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220271761 (NC_000006.12:26525636::A 8153/58078) Row 220271762 (NC_000006.12:26525636::AA 44/58682) Row 220271763 (NC_000006.12:26525636::AAA 3/58800)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 15104148 (NC_000006.12:26525640::A 265/1814) Row 15104149 (NC_000006.12:26525639:A: 268/1814) Row 15104150 (NC_000006.12:26525640::AA 20/1814)...	-	Apr 26, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 15104148 (NC_000006.12:26525640::A 265/1814) Row 15104149 (NC_000006.12:26525639:A: 268/1814) Row 15104150 (NC_000006.12:26525640::AA 20/1814)...	-	Apr 26, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 15104148 (NC_000006.12:26525640::A 265/1814) Row 15104149 (NC_000006.12:26525639:A: 268/1814) Row 15104150 (NC_000006.12:26525640::AA 20/1814)...	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 15104148 (NC_000006.12:26525640::A 265/1814) Row 15104149 (NC_000006.12:26525639:A: 268/1814) Row 15104150 (NC_000006.12:26525640::AA 20/1814)...	-	Apr 26, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 15104148 (NC_000006.12:26525640::A 265/1814) Row 15104149 (NC_000006.12:26525639:A: 268/1814) Row 15104150 (NC_000006.12:26525640::AA 20/1814)...	-	Apr 26, 2020 (154)
63	Northern Sweden	NC_000006.11 - 26525865	Jul 13, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 34630640 (NC_000006.11:26525864:A: 72/16748) Row 34630641 (NC_000006.11:26525864::A 373/16748) Row 34630642 (NC_000006.11:26525864::AA 3/16748)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 34630640 (NC_000006.11:26525864:A: 72/16748) Row 34630641 (NC_000006.11:26525864::A 373/16748) Row 34630642 (NC_000006.11:26525864::AA 3/16748)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 34630640 (NC_000006.11:26525864:A: 72/16748) Row 34630641 (NC_000006.11:26525864::A 373/16748) Row 34630642 (NC_000006.11:26525864::AA 3/16748)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 34630640 (NC_000006.11:26525864:A: 72/16748) Row 34630641 (NC_000006.11:26525864::A 373/16748) Row 34630642 (NC_000006.11:26525864::AA 3/16748)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 34630640 (NC_000006.11:26525864:A: 72/16748) Row 34630641 (NC_000006.11:26525864::A 373/16748) Row 34630642 (NC_000006.11:26525864::AA 3/16748)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 48306582 (NC_000006.12:26525636::A 553/28242) Row 48306583 (NC_000006.12:26525636:A: 101/28242) Row 48306584 (NC_000006.12:26525636::AA 2/28242)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 48306582 (NC_000006.12:26525636::A 553/28242) Row 48306583 (NC_000006.12:26525636:A: 101/28242) Row 48306584 (NC_000006.12:26525636::AA 2/28242)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 48306582 (NC_000006.12:26525636::A 553/28242) Row 48306583 (NC_000006.12:26525636:A: 101/28242) Row 48306584 (NC_000006.12:26525636::AA 2/28242)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 48306582 (NC_000006.12:26525636::A 553/28242) Row 48306583 (NC_000006.12:26525636:A: 101/28242) Row 48306584 (NC_000006.12:26525636::AA 2/28242)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 48306582 (NC_000006.12:26525636::A 553/28242) Row 48306583 (NC_000006.12:26525636:A: 101/28242) Row 48306584 (NC_000006.12:26525636::AA 2/28242)...	-	Oct 13, 2022 (156)
74	TopMed Submission ignored due to conflicting rows: Row 534721651 (NC_000006.12:26525636:AAAAAAA: 33/264690) Row 534721652 (NC_000006.12:26525636:AAAAAAAA: 2/264690) Row 534721653 (NC_000006.12:26525636:AAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
75	TopMed Submission ignored due to conflicting rows: Row 534721651 (NC_000006.12:26525636:AAAAAAA: 33/264690) Row 534721652 (NC_000006.12:26525636:AAAAAAAA: 2/264690) Row 534721653 (NC_000006.12:26525636:AAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
76	TopMed Submission ignored due to conflicting rows: Row 534721651 (NC_000006.12:26525636:AAAAAAA: 33/264690) Row 534721652 (NC_000006.12:26525636:AAAAAAAA: 2/264690) Row 534721653 (NC_000006.12:26525636:AAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
77	ALFA	NC_000006.12 - 26525637	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)
rs146461901	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4138802174, ss4697344095	NC_000006.12:26525636:AAAAAAAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4697344094	NC_000006.12:26525636:AAAAAAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4138802173, ss4697344093	NC_000006.12:26525636:AAAAAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4138802172	NC_000006.12:26525636:AAAAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5176661337	NC_000006.11:26525864:AAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3958726151, ss4138802171, ss5714469483	NC_000006.12:26525636:AAAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4138802170	NC_000006.12:26525636:AAA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss2998706589, ss3984331954	NC_000006.11:26525864:AA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4138802169, ss5267801387, ss5465558914	NC_000006.12:26525636:AA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3958726150	NC_000006.12:26525638:AA:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3785406237, ss3790767103, ss3795644446, ss3829797416, ss3986033769, ss5176661333	NC_000006.11:26525864:A:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5267801383, ss5465558911, ss5714469479	NC_000006.12:26525636:A:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3958726148	NC_000006.12:26525639:A:	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss295271117	NC_000006.10:26633844::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
6594036, ss3733309171, ss5176661334	NC_000006.11:26525864::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065074355, ss4138802166, ss5267801385, ss5465558913, ss5714469478	NC_000006.12:26525636::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3958726147	NC_000006.12:26525640::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss42718527	NT_007592.15:26465864::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss95950587	NT_007592.15:26465885::A	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5176661335	NC_000006.11:26525864::AA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4138802167, ss5267801386, ss5714469480	NC_000006.12:26525636::AA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3958726149	NC_000006.12:26525640::AA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4138802168, ss5465558915	NC_000006.12:26525636::AAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10408029367	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5176661336	NC_000006.11:26525864::AAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5714469481	NC_000006.12:26525636::AAAA	NC_000006.12:26525636:AAAAAAAAAAAA… NC_000006.12:26525636:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs35998206

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

rs35998206