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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
chr1:10816-10817 (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.

insA / insCA / insCG / insT
Variation Type
insCA=0.20469 (2428/11862, ALFA)
insCA=0.287 (90/314, 8.3KJPN)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DDX11L1 : 2KB Upstream 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.10816_10817insA
GRCh38.p13 chr 1 NC_000001.11:g.10816_10817insCA
GRCh38.p13 chr 1 NC_000001.11:g.10816_10817insCG
GRCh38.p13 chr 1 NC_000001.11:g.10816_10817insT
GRCh37.p13 chr 1 NC_000001.10:g.10816_10817insA
GRCh37.p13 chr 1 NC_000001.10:g.10816_10817insCA
GRCh37.p13 chr 1 NC_000001.10:g.10816_10817insCG
GRCh37.p13 chr 1 NC_000001.10:g.10816_10817insT
Gene: DDX11L1, DEAD/H-box helicase 11 like 1 (pseudogene) (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
DDX11L1 transcript NR_046018.2: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

ALFA Allele Frequency (New)
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 11862 =0.79531 CA=0.20469
European Sub 7618 =0.7990 CA=0.2010
African Sub 2816 =0.7873 CA=0.2127
African Others Sub 108 =0.815 CA=0.185
African American Sub 2708 =0.7862 CA=0.2138
Asian Sub 108 =0.685 CA=0.315
East Asian Sub 84 =0.70 CA=0.30
Other Asian Sub 24 =0.62 CA=0.38
Latin American 1 Sub 146 =0.699 CA=0.301
Latin American 2 Sub 610 =0.830 CA=0.170
South Asian Sub 94 =0.72 CA=0.28
Other Sub 470 =0.809 CA=0.191


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
8.3KJPN JAPANESE Study-wide 314 -

No frequency provided


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 = insA insCA insCG insT
GRCh38.p13 chr 1 NC_000001.11:g.10816_10817= NC_000001.11:g.10816_10817insA NC_000001.11:g.10816_10817insCA NC_000001.11:g.10816_10817insCG NC_000001.11:g.10816_10817insT
GRCh37.p13 chr 1 NC_000001.10:g.10816_10817= NC_000001.10:g.10816_10817insA NC_000001.10:g.10816_10817insCA NC_000001.10:g.10816_10817insCG NC_000001.10:g.10816_10817insT

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#.

6 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2750600986 Nov 08, 2017 (151)
2 SWEGEN ss2986141221 Nov 08, 2017 (151)
3 TOPMED ss3066316123 Nov 08, 2017 (151)
4 EVA_DECODE ss3685990281 Jul 12, 2019 (153)
5 EVA_DECODE ss3685990282 Jul 12, 2019 (153)
6 TOMMO_GENOMICS ss5142030922 Apr 25, 2021 (155)
7 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 558 (NC_000001.11:10816::A 2/2244)
Row 559 (NC_000001.11:10816::CA 901/2050)
Row 560 (NC_000001.11:10816::CG 3/2244)...

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

Submission ignored due to conflicting rows:
Row 558 (NC_000001.11:10816::A 2/2244)
Row 559 (NC_000001.11:10816::CA 901/2050)
Row 560 (NC_000001.11:10816::CG 3/2244)...

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

Submission ignored due to conflicting rows:
Row 558 (NC_000001.11:10816::A 2/2244)
Row 559 (NC_000001.11:10816::CA 901/2050)
Row 560 (NC_000001.11:10816::CG 3/2244)...

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

Submission ignored due to conflicting rows:
Row 558 (NC_000001.11:10816::A 2/2244)
Row 559 (NC_000001.11:10816::CA 901/2050)
Row 560 (NC_000001.11:10816::CG 3/2244)...

- Apr 25, 2021 (155)
11 8.3KJPN NC_000001.10 - 10817 Apr 25, 2021 (155)
12 ALFA NC_000001.11 - 10817 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
NC_000001.11:10816::A NC_000001.11:10816::A
229, ss2750600986, ss2986141221, ss5142030922 NC_000001.10:10816::CA NC_000001.11:10816::CA (self)
12069545334, ss3066316123, ss3685990281 NC_000001.11:10816::CA NC_000001.11:10816::CA (self)
ss3685990282 NC_000001.11:10816::CG NC_000001.11:10816::CG (self)
NC_000001.11:10816::T NC_000001.11:10816::T

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

No publications for rs1266288166


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