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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
chr1:3637054 (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.

Variation Type
SNV Single Nucleotide Variation
A=0.000034 (9/264690, TOPMED)
A=0.000016 (4/249884, GnomAD_exome)
A=0.000021 (3/140276, GnomAD) (+ 3 more)
A=0.000009 (1/111722, ExAC)
A=0.00000 (0/14050, ALFA)
A=0.00008 (1/13004, GO-ESP)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
WRAP73 : Missense 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.3637054G>A
GRCh37.p13 chr 1 NC_000001.10:g.3553618G>A
WRAP73 RefSeqGene NG_033937.1:g.18054C>T
Gene: WRAP73, WD repeat containing, antisense to TP73 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
WRAP73 transcript NM_017818.4:c.457C>T R [CGG] > W [TGG] Coding Sequence Variant
WD repeat-containing protein WRAP73 NP_060288.3:p.Arg153Trp R (Arg) > W (Trp) Missense Variant
WRAP73 transcript variant X1 XM_017001387.2:c.457C>T R [CGG] > W [TGG] Coding Sequence Variant
WD repeat-containing protein WRAP73 isoform X1 XP_016856876.1:p.Arg153Trp R (Arg) > W (Trp) Missense Variant
WRAP73 transcript variant X2 XM_005244754.2:c.457C>T R [CGG] > W [TGG] Coding Sequence Variant
WD repeat-containing protein WRAP73 isoform X2 XP_005244811.1:p.Arg153Trp R (Arg) > W (Trp) Missense Variant
WRAP73 transcript variant X3 XR_946661.3:n.523C>T 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

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
European Sub 9690 G=1.0000 A=0.0000
African Sub 2898 G=1.0000 A=0.0000
African Others Sub 114 G=1.000 A=0.000
African American Sub 2784 G=1.0000 A=0.0000
Asian Sub 112 G=1.000 A=0.000
East Asian Sub 86 G=1.00 A=0.00
Other Asian Sub 26 G=1.00 A=0.00
Latin American 1 Sub 146 G=1.000 A=0.000
Latin American 2 Sub 610 G=1.000 A=0.000
South Asian Sub 98 G=1.00 A=0.00
Other Sub 496 G=1.000 A=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
TopMed Global Study-wide 264690 G=0.999966 A=0.000034
gnomAD - Exomes Global Study-wide 249884 G=0.999984 A=0.000016
gnomAD - Exomes European Sub 134306 G=0.999978 A=0.000022
gnomAD - Exomes Asian Sub 48876 G=0.99998 A=0.00002
gnomAD - Exomes American Sub 34524 G=1.00000 A=0.00000
gnomAD - Exomes African Sub 16096 G=1.00000 A=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 9998 G=1.0000 A=0.0000
gnomAD - Exomes Other Sub 6084 G=1.0000 A=0.0000
gnomAD - Genomes Global Study-wide 140276 G=0.999979 A=0.000021
gnomAD - Genomes European Sub 75962 G=0.99997 A=0.00003
gnomAD - Genomes African Sub 42044 G=0.99998 A=0.00002
gnomAD - Genomes American Sub 13662 G=1.00000 A=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3132 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2154 G=1.0000 A=0.0000
ExAC Global Study-wide 111722 G=0.999991 A=0.000009
ExAC Europe Sub 67458 G=1.00000 A=0.00000
ExAC Asian Sub 23294 G=0.99996 A=0.00004
ExAC American Sub 10770 G=1.00000 A=0.00000
ExAC African Sub 9378 G=1.0000 A=0.0000
ExAC Other Sub 822 G=1.000 A=0.000
GO Exome Sequencing Project Global Study-wide 13004 G=0.99992 A=0.00008
GO Exome Sequencing Project European American Sub 8598 G=0.9999 A=0.0001
GO Exome Sequencing Project African American Sub 4406 G=1.0000 A=0.0000

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
GRCh38.p13 chr 1 NC_000001.11:g.3637054= NC_000001.11:g.3637054G>A
GRCh37.p13 chr 1 NC_000001.10:g.3553618= NC_000001.10:g.3553618G>A
WRAP73 RefSeqGene NG_033937.1:g.18054= NG_033937.1:g.18054C>T
WRAP73 transcript NM_017818.4:c.457= NM_017818.4:c.457C>T
WRAP73 transcript NM_017818.3:c.457= NM_017818.3:c.457C>T
WRAP73 transcript variant X3 XR_946661.3:n.523= XR_946661.3:n.523C>T
WRAP73 transcript variant X1 XM_017001387.2:c.457= XM_017001387.2:c.457C>T
WRAP73 transcript variant X2 XM_005244754.2:c.457= XM_005244754.2:c.457C>T
WRAP73 transcript variant X2 XM_005244754.1:c.457= XM_005244754.1:c.457C>T
WD repeat-containing protein WRAP73 NP_060288.3:p.Arg153= NP_060288.3:p.Arg153Trp
WD repeat-containing protein WRAP73 isoform X1 XP_016856876.1:p.Arg153= XP_016856876.1:p.Arg153Trp
WD repeat-containing protein WRAP73 isoform X2 XP_005244811.1:p.Arg153= XP_005244811.1:p.Arg153Trp

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#.

8 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss217392083 Jul 14, 2010 (132)
2 NHLBI-ESP ss712267192 Apr 25, 2013 (138)
3 EVA_EXAC ss1685260473 Apr 01, 2015 (144)
4 GNOMAD ss2731054880 Nov 08, 2017 (151)
5 TOPMED ss3067088514 Nov 08, 2017 (151)
6 EVA ss3823550307 Apr 25, 2020 (154)
7 GNOMAD ss3987347598 Apr 25, 2021 (155)
8 TOPMED ss4437255512 Apr 25, 2021 (155)
9 ExAC NC_000001.10 - 3553618 Oct 11, 2018 (152)
10 gnomAD - Genomes NC_000001.11 - 3637054 Apr 25, 2021 (155)
11 gnomAD - Exomes NC_000001.10 - 3553618 Jul 12, 2019 (153)
12 GO Exome Sequencing Project NC_000001.10 - 3553618 Oct 11, 2018 (152)
13 TopMed NC_000001.11 - 3637054 Apr 25, 2021 (155)
14 ALFA NC_000001.11 - 3637054 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
ss217392083 NC_000001.9:3543477:G:A NC_000001.11:3637053:G:A (self)
4436712, 69838, 9041, ss712267192, ss1685260473, ss2731054880, ss3823550307 NC_000001.10:3553617:G:A NC_000001.11:3637053:G:A (self)
821800, 535690, 861847, 11191395231, ss3067088514, ss3987347598, ss4437255512 NC_000001.11:3637053:G:A NC_000001.11:3637053:G:A (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 rs114959668


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