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dbSNP Short Genetic Variations

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.


Current Build 155

Released April 9, 2021

Homo sapiens
chr1:930354 (GRCh38.p13) 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.

G>A / G>T
Variation Type
SNV Single Nucleotide Variation
A=0.000068 (14/204508, GnomAD_exome)
A=0.00000 (0/14050, ALFA)
T=0.00000 (0/14050, ALFA) (+ 1 more)
A=0.0004 (2/5008, 1000G)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SAMD11 : Intron Variant
0 citations
Genomic View
See rs on genome

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.p13 chr 1 NC_000001.11:g.930354G>A
GRCh38.p13 chr 1 NC_000001.11:g.930354G>T
GRCh37.p13 chr 1 NC_000001.10:g.865734G>A
GRCh37.p13 chr 1 NC_000001.10:g.865734G>T
Gene: SAMD11, sterile alpha motif domain containing 11 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SAMD11 transcript variant 2 NM_001385640.1:c.791+18G>A N/A Intron Variant
SAMD11 transcript variant 1 NM_001385641.1:c.791+18G>A N/A Intron Variant
SAMD11 transcript variant 3 NM_152486.4:c.254+18G>A N/A Intron Variant

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

Not Reported in ClinVar

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 14050 G=1.00000 A=0.00000, T=0.00000
European Sub 9690 G=1.0000 A=0.0000, T=0.0000
African Sub 2898 G=1.0000 A=0.0000, T=0.0000
African Others Sub 114 G=1.000 A=0.000, T=0.000
African American Sub 2784 G=1.0000 A=0.0000, T=0.0000
Asian Sub 112 G=1.000 A=0.000, T=0.000
East Asian Sub 86 G=1.00 A=0.00, T=0.00
Other Asian Sub 26 G=1.00 A=0.00, T=0.00
Latin American 1 Sub 146 G=1.000 A=0.000, T=0.000
Latin American 2 Sub 610 G=1.000 A=0.000, T=0.000
South Asian Sub 98 G=1.00 A=0.00, T=0.00
Other Sub 496 G=1.000 A=0.000, T=0.000


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").

Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 204508 G=0.999932 A=0.000068
gnomAD - Exomes European Sub 106342 G=0.999962 A=0.000038
gnomAD - Exomes Asian Sub 41580 G=0.99976 A=0.00024
gnomAD - Exomes American Sub 29750 G=1.00000 A=0.00000
gnomAD - Exomes African Sub 12570 G=1.00000 A=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 9038 G=1.0000 A=0.0000
gnomAD - Exomes Other Sub 5228 G=1.0000 A=0.0000
1000Genomes Global Study-wide 5008 G=0.9996 A=0.0004
1000Genomes African Sub 1322 G=1.0000 A=0.0000
1000Genomes East Asian Sub 1008 G=0.9990 A=0.0010
1000Genomes Europe Sub 1006 G=1.0000 A=0.0000
1000Genomes South Asian Sub 978 G=0.999 A=0.001
1000Genomes American Sub 694 G=1.000 A=0.000

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 G= A T
GRCh38.p13 chr 1 NC_000001.11:g.930354= NC_000001.11:g.930354G>A NC_000001.11:g.930354G>T
GRCh37.p13 chr 1 NC_000001.10:g.865734= NC_000001.10:g.865734G>A NC_000001.10:g.865734G>T
SAMD11 transcript variant 2 NM_001385640.1:c.791+18= NM_001385640.1:c.791+18G>A NM_001385640.1:c.791+18G>T
SAMD11 transcript variant 1 NM_001385641.1:c.791+18= NM_001385641.1:c.791+18G>A NM_001385641.1:c.791+18G>T
SAMD11 transcript NM_152486.2:c.254+18= NM_152486.2:c.254+18G>A NM_152486.2:c.254+18G>T
SAMD11 transcript variant 3 NM_152486.4:c.254+18= NM_152486.4:c.254+18G>A NM_152486.4:c.254+18G>T
SAMD11 transcript variant X1 XM_005244723.1:c.254+18= XM_005244723.1:c.254+18G>A XM_005244723.1:c.254+18G>T
SAMD11 transcript variant X2 XM_005244724.1:c.254+18= XM_005244724.1:c.254+18G>A XM_005244724.1:c.254+18G>T
SAMD11 transcript variant X3 XM_005244725.1:c.254+18= XM_005244725.1:c.254+18G>A XM_005244725.1:c.254+18G>T
SAMD11 transcript variant X4 XM_005244726.1:c.254+18= XM_005244726.1:c.254+18G>A XM_005244726.1:c.254+18G>T
SAMD11 transcript variant X5 XM_005244727.1:c.254+18= XM_005244727.1:c.254+18G>A XM_005244727.1:c.254+18G>T

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#.

13 SubSNP, 9 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss487561407 May 04, 2012 (137)
2 1000GENOMES ss1289342548 Aug 21, 2014 (142)
3 EVA_EXAC ss1685217325 Apr 01, 2015 (144)
4 EVA_EXAC ss1685217326 Apr 01, 2015 (144)
5 GNOMAD ss2730986947 Nov 08, 2017 (151)
6 GNOMAD ss2746169462 Nov 08, 2017 (151)
7 GNOMAD ss2750649392 Nov 08, 2017 (151)
8 TOPMED ss3066421353 Nov 08, 2017 (151)
9 TOPMED ss3066421354 Nov 08, 2017 (151)
10 OMUKHERJEE_ADBS ss3646218742 Oct 11, 2018 (152)
11 EVA ss3745721936 Jul 12, 2019 (153)
12 TOPMED ss4436458196 Apr 25, 2021 (155)
13 TOPMED ss4436458197 Apr 25, 2021 (155)
14 1000Genomes NC_000001.10 - 865734 Oct 11, 2018 (152)
15 ExAC

Submission ignored due to conflicting rows:
Row 4390429 (NC_000001.10:865733:G:G 50108/50114, NC_000001.10:865733:G:A 6/50114)
Row 4390430 (NC_000001.10:865733:G:G 50114/50114, NC_000001.10:865733:G:T 0/50114)

- Oct 11, 2018 (152)
16 ExAC

Submission ignored due to conflicting rows:
Row 4390429 (NC_000001.10:865733:G:G 50108/50114, NC_000001.10:865733:G:A 6/50114)
Row 4390430 (NC_000001.10:865733:G:G 50114/50114, NC_000001.10:865733:G:T 0/50114)

- Oct 11, 2018 (152)
17 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 87263 (NC_000001.11:930353:G:A 5/140272)
Row 87264 (NC_000001.11:930353:G:T 3/140272)

- Apr 25, 2021 (155)
18 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 87263 (NC_000001.11:930353:G:A 5/140272)
Row 87264 (NC_000001.11:930353:G:T 3/140272)

- Apr 25, 2021 (155)
19 gnomAD - Exomes NC_000001.10 - 865734 Jul 12, 2019 (153)
20 TopMed

Submission ignored due to conflicting rows:
Row 64531 (NC_000001.11:930353:G:A 11/264690)
Row 64532 (NC_000001.11:930353:G:T 7/264690)

- Apr 25, 2021 (155)
21 TopMed

Submission ignored due to conflicting rows:
Row 64531 (NC_000001.11:930353:G:A 11/264690)
Row 64532 (NC_000001.11:930353:G:T 7/264690)

- Apr 25, 2021 (155)
22 ALFA NC_000001.11 - 930354 Apr 25, 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
7407, 1285, ss487561407, ss1289342548, ss1685217325, ss2730986947, ss2746169462, ss2750649392, ss3646218742, ss3745721936 NC_000001.10:865733:G:A NC_000001.11:930353:G:A (self)
32475, 4906042225, ss3066421353, ss4436458196 NC_000001.11:930353:G:A NC_000001.11:930353:G:A (self)
ss1685217326, ss2730986947 NC_000001.10:865733:G:T NC_000001.11:930353:G:T (self)
32475, 4906042225, ss3066421354, ss4436458197 NC_000001.11:930353:G:T NC_000001.11:930353:G:T (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 rs201326364


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.

Software version is: 2.0.1.post596+ae089ad