Name: rs10649975
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.

rs10649975

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:88187716-88187734 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / ins(T)₄C(T)₅GTCTGC(T)₁₉ / dup(T)₅ / dup(T)₈ / dup(T)₉ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₇ / dup(T)₁₉
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.3698 (1852/5008, 1000G)
(T)₁₉=0.3027 (1367/4516, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF469 : Intron Variant
LOC105371401 : 2KB Upstream 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	4516	TTTTTTTTTTTTTTTTTTT=0.3027	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0040, TTTTTTTTTTTTTTTTTT=0.3202, TTTTTTTTTTTTTTTTTTTTTT=0.0740, TTTTTTTTTTTTTTTTTTTTT=0.2865, TTTTTTTTTTTTTTTTTTTT=0.0109, TTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.484762	0.279048	0.23619	32
European	Sub	4424	TTTTTTTTTTTTTTTTTTT=0.2900	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0041, TTTTTTTTTTTTTTTTTT=0.3262, TTTTTTTTTTTTTTTTTTTTTT=0.0750, TTTTTTTTTTTTTTTTTTTTT=0.2918, TTTTTTTTTTTTTTTTTTTT=0.0111, TTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.463754	0.28997	0.246276	32
African	Sub	64	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	62	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	12	TTTTTTTTTTTTTTTTTTT=0.33	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.25, TTTTTTTTTTTTTTTTTTTTTT=0.17, TTTTTTTTTTTTTTTTTTTTT=0.25, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.666667	0.333333	0.0	2

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
1000Genomes	Global	Study-wide	5008	(T)₁₉=0.6302	delTT=0.3698
1000Genomes	African	Sub	1322	(T)₁₉=0.7201	delTT=0.2799
1000Genomes	East Asian	Sub	1008	(T)₁₉=0.5317	delTT=0.4683
1000Genomes	Europe	Sub	1006	(T)₁₉=0.6978	delTT=0.3022
1000Genomes	South Asian	Sub	978	(T)₁₉=0.521	delTT=0.479
1000Genomes	American	Sub	694	(T)₁₉=0.657	delTT=0.343
Allele Frequency Aggregator	Total	Global	4516	(T)₁₉=0.3027	del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0040, delT=0.3202, dupT=0.0109, dupTT=0.2865, dupTTT=0.0740, dup(T)₄=0.0018, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	4424	(T)₁₉=0.2900	del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0041, delT=0.3262, dupT=0.0111, dupTT=0.2918, dupTTT=0.0750, dup(T)₄=0.0018, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	64	(T)₁₉=1.00	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, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(T)₁₉=1.00	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, dup(T)₅=0.00
Allele Frequency Aggregator	Other	Sub	12	(T)₁₉=0.33	del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.25, dupT=0.00, dupTT=0.25, dupTTT=0.17, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₁₉=1.0	del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₉=0	del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₉=0	del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 16	NC_000016.10:g.88187729_88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187730_88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187731_88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187732_88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187733_88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187734del
GRCh38.p14 chr 16	NC_000016.10:g.88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187733_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187732_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187731_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187716_88187734T[23]CTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 16	NC_000016.10:g.88187730_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187727_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187726_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187723_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187722_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187721_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187720_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187718_88187734dup
GRCh38.p14 chr 16	NC_000016.10:g.88187716_88187734dup
GRCh37.p13 chr 16	NC_000016.9:g.88221335_88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221336_88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221337_88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221338_88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221339_88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221340del
GRCh37.p13 chr 16	NC_000016.9:g.88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221339_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221338_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221337_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221322_88221340T[23]CTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 16	NC_000016.9:g.88221336_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221333_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221332_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221329_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221328_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221327_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221326_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221324_88221340dup
GRCh37.p13 chr 16	NC_000016.9:g.88221322_88221340dup

Gene: ZNF469, zinc finger protein 469 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF469 transcript	NM_001367624.2:c.	N/A	Genic Upstream Transcript Variant
ZNF469 transcript variant X1	XM_047434810.1:c.-294+866… XM_047434810.1:c.-294+86660_-294+86665del	N/A	Intron Variant

Gene: LOC105371401, uncharacterized LOC105371401 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105371401 transcript variant X1	XR_007065176.1:n.	N/A	Upstream Transcript Variant
LOC105371401 transcript variant X2	XR_007065177.1:n.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₉=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	ins(T)₄C(T)₅GTCTGC(T)₁₉	dup(T)₅	dup(T)₈	dup(T)₉	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₇	dup(T)₁₉
GRCh38.p14 chr 16	NC_000016.10:g.88187716_88187734=	NC_000016.10:g.88187729_88187734del	NC_000016.10:g.88187730_88187734del	NC_000016.10:g.88187731_88187734del	NC_000016.10:g.88187732_88187734del	NC_000016.10:g.88187733_88187734del	NC_000016.10:g.88187734del	NC_000016.10:g.88187734dup	NC_000016.10:g.88187733_88187734dup	NC_000016.10:g.88187732_88187734dup	NC_000016.10:g.88187731_88187734dup	NC_000016.10:g.88187716_88187734T[23]CTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT[1]	NC_000016.10:g.88187730_88187734dup	NC_000016.10:g.88187727_88187734dup	NC_000016.10:g.88187726_88187734dup	NC_000016.10:g.88187723_88187734dup	NC_000016.10:g.88187722_88187734dup	NC_000016.10:g.88187721_88187734dup	NC_000016.10:g.88187720_88187734dup	NC_000016.10:g.88187718_88187734dup	NC_000016.10:g.88187716_88187734dup
GRCh37.p13 chr 16	NC_000016.9:g.88221322_88221340=	NC_000016.9:g.88221335_88221340del	NC_000016.9:g.88221336_88221340del	NC_000016.9:g.88221337_88221340del	NC_000016.9:g.88221338_88221340del	NC_000016.9:g.88221339_88221340del	NC_000016.9:g.88221340del	NC_000016.9:g.88221340dup	NC_000016.9:g.88221339_88221340dup	NC_000016.9:g.88221338_88221340dup	NC_000016.9:g.88221337_88221340dup	NC_000016.9:g.88221322_88221340T[23]CTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT[1]	NC_000016.9:g.88221336_88221340dup	NC_000016.9:g.88221333_88221340dup	NC_000016.9:g.88221332_88221340dup	NC_000016.9:g.88221329_88221340dup	NC_000016.9:g.88221328_88221340dup	NC_000016.9:g.88221327_88221340dup	NC_000016.9:g.88221326_88221340dup	NC_000016.9:g.88221324_88221340dup	NC_000016.9:g.88221322_88221340dup
ZNF469 transcript variant X1	XM_047434810.1:c.-294+86647=	XM_047434810.1:c.-294+86660_-294+86665del	XM_047434810.1:c.-294+86661_-294+86665del	XM_047434810.1:c.-294+86662_-294+86665del	XM_047434810.1:c.-294+86663_-294+86665del	XM_047434810.1:c.-294+86664_-294+86665del	XM_047434810.1:c.-294+86665del	XM_047434810.1:c.-294+86665dup	XM_047434810.1:c.-294+86664_-294+86665dup	XM_047434810.1:c.-294+86663_-294+86665dup	XM_047434810.1:c.-294+86662_-294+86665dup	XM_047434810.1:c.-294+86665_-294+86666insTTTTCTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT	XM_047434810.1:c.-294+86661_-294+86665dup	XM_047434810.1:c.-294+86658_-294+86665dup	XM_047434810.1:c.-294+86657_-294+86665dup	XM_047434810.1:c.-294+86654_-294+86665dup	XM_047434810.1:c.-294+86653_-294+86665dup	XM_047434810.1:c.-294+86652_-294+86665dup	XM_047434810.1:c.-294+86651_-294+86665dup	XM_047434810.1:c.-294+86649_-294+86665dup	XM_047434810.1:c.-294+86647_-294+86665dup

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#.

77 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80124606	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95684987	Dec 05, 2013 (138)
3	HUMANGENOME_JCVI	ss96716932	Mar 15, 2016 (147)
4	GMI	ss289309695	Oct 12, 2018 (152)
5	PJP	ss294900232	May 09, 2011 (137)
6	1000GENOMES	ss1376218938	Oct 12, 2018 (152)
7	EVA_UK10K_ALSPAC	ss1708646059	Oct 12, 2018 (152)
8	EVA_UK10K_TWINSUK	ss1708646563	Oct 12, 2018 (152)
9	EVA_UK10K_ALSPAC	ss1710715099	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710715100	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710715101	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710715102	Apr 01, 2015 (144)
13	SWEGEN	ss3015010955	Nov 17, 2017 (151)
14	URBANLAB	ss3650575820	Oct 12, 2018 (152)
15	EVA_DECODE	ss3699867924	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699867925	Jul 13, 2019 (153)
17	EVA_DECODE	ss3699867926	Jul 13, 2019 (153)
18	EVA_DECODE	ss3699867927	Jul 13, 2019 (153)
19	EVA_DECODE	ss3699867928	Jul 13, 2019 (153)
20	EVA_DECODE	ss3699867929	Jul 13, 2019 (153)
21	ACPOP	ss3741775872	Jul 13, 2019 (153)
22	ACPOP	ss3741775873	Jul 13, 2019 (153)
23	ACPOP	ss3741775874	Jul 13, 2019 (153)
24	ACPOP	ss3741775875	Jul 13, 2019 (153)
25	ACPOP	ss3741775876	Jul 13, 2019 (153)
26	ACPOP	ss3741775877	Jul 13, 2019 (153)
27	PACBIO	ss3793090683	Jul 13, 2019 (153)
28	PACBIO	ss3793090684	Jul 13, 2019 (153)
29	PACBIO	ss3797976051	Jul 13, 2019 (153)
30	PACBIO	ss3797976052	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3819591587	Jul 13, 2019 (153)
32	EVA	ss3834723600	Apr 27, 2020 (154)
33	GNOMAD	ss4306194788	Apr 27, 2021 (155)
34	GNOMAD	ss4306194789	Apr 27, 2021 (155)
35	GNOMAD	ss4306194790	Apr 27, 2021 (155)
36	GNOMAD	ss4306194791	Apr 27, 2021 (155)
37	GNOMAD	ss4306194792	Apr 27, 2021 (155)
38	GNOMAD	ss4306194793	Apr 27, 2021 (155)
39	GNOMAD	ss4306194794	Apr 27, 2021 (155)
40	GNOMAD	ss4306194795	Apr 27, 2021 (155)
41	GNOMAD	ss4306194796	Apr 27, 2021 (155)
42	GNOMAD	ss4306194797	Apr 27, 2021 (155)
43	GNOMAD	ss4306194799	Apr 27, 2021 (155)
44	GNOMAD	ss4306194800	Apr 27, 2021 (155)
45	GNOMAD	ss4306194801	Apr 27, 2021 (155)
46	GNOMAD	ss4306194802	Apr 27, 2021 (155)
47	GNOMAD	ss4306194803	Apr 27, 2021 (155)
48	GNOMAD	ss4306194804	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5220973098	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5220973099	Apr 27, 2021 (155)
51	TOMMO_GENOMICS	ss5220973100	Apr 27, 2021 (155)
52	TOMMO_GENOMICS	ss5220973101	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5220973102	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5220973103	Apr 27, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5302038014	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5302038015	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5302038016	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5302038017	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5302038018	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5302038019	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5495271380	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5495271381	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5495271382	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5495271383	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5495271384	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5495271385	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5776390190	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5776390191	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5776390192	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5776390193	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5776390194	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5776390195	Oct 16, 2022 (156)
73	EVA	ss5846832737	Oct 16, 2022 (156)
74	EVA	ss5846832738	Oct 16, 2022 (156)
75	EVA	ss5846832739	Oct 16, 2022 (156)
76	EVA	ss5851695206	Oct 16, 2022 (156)
77	EVA	ss5900330181	Oct 16, 2022 (156)
78	1000Genomes	NC_000016.9 - 88221322	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1494/3854) Row 39218808 (NC_000016.9:88221321::TT 2044/3854) Row 39218809 (NC_000016.9:88221321::TTT 298/3854)	-	Oct 12, 2018 (152)
80	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1494/3854) Row 39218808 (NC_000016.9:88221321::TT 2044/3854) Row 39218809 (NC_000016.9:88221321::TTT 298/3854)	-	Oct 12, 2018 (152)
81	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1494/3854) Row 39218808 (NC_000016.9:88221321::TT 2044/3854) Row 39218809 (NC_000016.9:88221321::TTT 298/3854)	-	Oct 12, 2018 (152)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 498462281 (NC_000016.10:88187715::T 9131/128854) Row 498462282 (NC_000016.10:88187715::TT 33949/128804) Row 498462283 (NC_000016.10:88187715::TTT 15272/128806)...	-	Apr 27, 2021 (155)
98	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
99	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
100	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
101	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
102	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 15060737 (NC_000016.9:88221321:T: 177/594) Row 15060738 (NC_000016.9:88221321::TTT 48/594) Row 15060739 (NC_000016.9:88221321::TT 132/594)...	-	Jul 13, 2019 (153)
104	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 78942405 (NC_000016.9:88221321:T: 12502/16632) Row 78942406 (NC_000016.9:88221321::TTT 765/16632) Row 78942407 (NC_000016.9:88221321::TT 2259/16632)...	-	Apr 27, 2021 (155)
110	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 110227294 (NC_000016.10:88187715:T: 21457/28238) Row 110227295 (NC_000016.10:88187715::TTT 1375/28238) Row 110227296 (NC_000016.10:88187715::TT 4016/28238)...	-	Oct 16, 2022 (156)
116	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1443/3708) Row 39218808 (NC_000016.9:88221321::TT 1982/3708) Row 39218809 (NC_000016.9:88221321::TTT 269/3708)	-	Oct 12, 2018 (152)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1443/3708) Row 39218808 (NC_000016.9:88221321::TT 1982/3708) Row 39218809 (NC_000016.9:88221321::TTT 269/3708)	-	Oct 12, 2018 (152)
118	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39218807 (NC_000016.9:88221321:TT: 1443/3708) Row 39218808 (NC_000016.9:88221321::TT 1982/3708) Row 39218809 (NC_000016.9:88221321::TTT 269/3708)	-	Oct 12, 2018 (152)
119	ALFA	NC_000016.10 - 88187716	Apr 27, 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)
rs71391379	May 11, 2012 (137)
rs63700461	May 11, 2012 (137)
rs71158709	May 11, 2012 (137)
rs71888730	May 11, 2012 (137)
rs72232733	May 11, 2012 (137)
rs146013276	Sep 17, 2011 (135)
rs538203004	Apr 01, 2015 (144)
rs796131377	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4306194804	NC_000016.10:88187715:TTTTTT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4306194803	NC_000016.10:88187715:TTTTT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4306194802, ss5900330181	NC_000016.10:88187715:TTTT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4306194801, ss5302038019, ss5495271385	NC_000016.10:88187715:TTT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss289309695	NC_000016.8:86778822:TT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
70685553, ss1376218938, ss1708646059, ss1708646563, ss3015010955, ss5220973101, ss5846832739	NC_000016.9:88221321:TT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3650575820, ss3699867924, ss3819591587, ss4306194800, ss5302038017, ss5495271380, ss5776390194	NC_000016.10:88187715:TT:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss80124606	NC_000016.8:86778840:T:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3741775872, ss3834723600, ss5220973098	NC_000016.9:88221321:T:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4306194799, ss5302038014, ss5495271381, ss5776390190, ss5851695206	NC_000016.10:88187715:T:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3699867925	NC_000016.10:88187716:T:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss96716932	NT_010498.15:41835520:T:	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5220973102	NC_000016.9:88221321::T	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4306194788, ss5302038016, ss5495271382, ss5776390193	NC_000016.10:88187715::T	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3699867926	NC_000016.10:88187717::T	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294900232	NC_000016.8:86778823::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3741775874, ss3793090683, ss3797976051, ss5220973100, ss5846832737	NC_000016.9:88221321::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1710715099, ss1710715100	NC_000016.9:88221323::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194789, ss5302038018, ss5495271383, ss5776390192	NC_000016.10:88187715::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3699867927	NC_000016.10:88187717::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss96716932	NT_010498.15:41835520:T:TTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95684987	NT_010498.15:41835539::TT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3741775873, ss3793090684, ss3797976052, ss5220973099, ss5846832738	NC_000016.9:88221321::TTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710715101, ss1710715102	NC_000016.9:88221323::TTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194790, ss5302038015, ss5495271384, ss5776390191	NC_000016.10:88187715::TTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3699867928	NC_000016.10:88187717::TTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5220973103	NC_000016.9:88221321::TTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194791, ss5776390195	NC_000016.10:88187715::TTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194797	NC_000016.10:88187715::TTTTTTTTTTT… NC_000016.10:88187715::TTTTTTTTTTTTTTTTTTTTTTTCTTTTTGTCTGC	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTGTCTGCTTTTTTTTTTTTTTTTTTT	(self)
ss4306194792	NC_000016.10:88187715::TTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10100848895	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194793	NC_000016.10:88187715::TTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194794	NC_000016.10:88187715::TTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194795	NC_000016.10:88187715::TTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741775875	NC_000016.9:88221321::TTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3699867929	NC_000016.10:88187717::TTTTTTTTTTT… NC_000016.10:88187717::TTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741775876	NC_000016.9:88221321::TTTTTTTTTTTT… NC_000016.9:88221321::TTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4306194796	NC_000016.10:88187715::TTTTTTTTTTT… NC_000016.10:88187715::TTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741775877	NC_000016.9:88221321::TTTTTTTTTTTT… NC_000016.9:88221321::TTTTTTTTTTTTTTTTTTT	NC_000016.10:88187715:TTTTTTTTTTTT… NC_000016.10:88187715:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs10649975

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

rs10649975