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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1489537336

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:49556579 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000004 (1/264690, TOPMED)
A=0.000007 (1/140234, GnomAD)
A=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
C6orf141 : Intron 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 14050 G=1.00000 A=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 G=1.000 A=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 G=1.000 A=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 G=1.000 A=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 G=1.000 A=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Sub 496 G=1.000 A=0.000 1.0 0.0 0.0 N/A


Help

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
TopMed Global Study-wide 264690 G=0.999996 A=0.000004
gnomAD - Genomes Global Study-wide 140234 G=0.999993 A=0.000007
gnomAD - Genomes European Sub 75960 G=1.00000 A=0.00000
gnomAD - Genomes African Sub 42020 G=0.99998 A=0.00002
gnomAD - Genomes American Sub 13646 G=1.00000 A=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3132 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=1.0000 A=0.0000
Allele Frequency Aggregator Total Global 14050 G=1.00000 A=0.00000
Allele Frequency Aggregator European Sub 9690 G=1.0000 A=0.0000
Allele Frequency Aggregator African Sub 2898 G=1.0000 A=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 G=1.000 A=0.000
Allele Frequency Aggregator Other Sub 496 G=1.000 A=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=1.000 A=0.000
Allele Frequency Aggregator Asian Sub 112 G=1.000 A=0.000
Allele Frequency Aggregator South Asian Sub 98 G=1.00 A=0.00
Help

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.49556579G>A
GRCh37.p13 chr 6 NC_000006.11:g.49524292G>A
Gene: C6orf141, chromosome 6 open reading frame 141 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
C6orf141 transcript variant 1 NM_001145652.2:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant 2 NR_146853.2:n. N/A Intron Variant
C6orf141 transcript variant 3 NR_146854.3:n. N/A Intron Variant
C6orf141 transcript variant 4 NR_146855.2:n. N/A Intron Variant
C6orf141 transcript variant 5 NR_146856.3:n. N/A Intron Variant
C6orf141 transcript variant 6 NR_146857.3:n. N/A Intron Variant
C6orf141 transcript variant 7 NR_146858.2:n. N/A Intron Variant
C6orf141 transcript variant 8 NR_146859.3:n. N/A Intron Variant
C6orf141 transcript variant 9 NR_146860.3:n. N/A Intron Variant
C6orf141 transcript variant 10 NR_146861.2:n. N/A Intron Variant
C6orf141 transcript variant 11 NR_146862.3:n. N/A Intron Variant
C6orf141 transcript variant 12 NR_146863.2:n. N/A Intron Variant
C6orf141 transcript variant 13 NR_146864.3:n. N/A Intron Variant
C6orf141 transcript NR_170563.1:n. N/A Intron Variant
C6orf141 transcript NR_170564.1:n. N/A Intron Variant
C6orf141 transcript NR_170565.1:n. N/A Intron Variant
C6orf141 transcript NR_170566.1:n. N/A Intron Variant
C6orf141 transcript NR_170567.1:n. N/A Intron Variant
C6orf141 transcript NR_170568.1:n. N/A Intron Variant
C6orf141 transcript NR_170569.1:n. N/A Intron Variant
C6orf141 transcript NR_170570.1:n. N/A Intron Variant
C6orf141 transcript NR_170571.1:n. N/A Intron Variant
C6orf141 transcript NR_170572.1:n. N/A Intron Variant
C6orf141 transcript NR_170573.1:n. N/A Intron Variant
C6orf141 transcript NR_170574.1:n. N/A Intron Variant
C6orf141 transcript NR_170575.1:n. N/A Intron Variant
C6orf141 transcript NR_170576.1:n. N/A Intron Variant
C6orf141 transcript NR_170577.1:n. N/A Intron Variant
C6orf141 transcript NR_170578.1:n. N/A Intron Variant
C6orf141 transcript NR_170579.1:n. N/A Intron Variant
C6orf141 transcript NR_170580.1:n. N/A Intron Variant
C6orf141 transcript NR_170581.1:n. N/A Intron Variant
C6orf141 transcript NR_170582.1:n. N/A Intron Variant
C6orf141 transcript NR_170583.1:n. N/A Intron Variant
C6orf141 transcript NR_170584.1:n. N/A Intron Variant
C6orf141 transcript NR_170585.1:n. N/A Intron Variant
C6orf141 transcript NR_170586.1:n. N/A Intron Variant
C6orf141 transcript NR_170587.1:n. N/A Intron Variant
C6orf141 transcript NR_170588.1:n. N/A Intron Variant
C6orf141 transcript NR_170589.1:n. N/A Intron Variant
C6orf141 transcript NR_170590.1:n. N/A Intron Variant
C6orf141 transcript NR_170591.1:n. N/A Intron Variant
C6orf141 transcript NR_170592.1:n. N/A Intron Variant
C6orf141 transcript NR_170593.1:n. N/A Intron Variant
C6orf141 transcript variant X4 XM_047418226.1:c.*3019+14…

XM_047418226.1:c.*3019+1422G>A

 		N/A Intron Variant
C6orf141 transcript variant X6 XM_047418229.1:c.*3124+14…

XM_047418229.1:c.*3124+1422G>A

 		N/A Intron Variant
C6orf141 transcript variant X8 XM_047418230.1:c.*666+142…

XM_047418230.1:c.*666+1422G>A

 		N/A Intron Variant
C6orf141 transcript variant X1 XM_005248850.4:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X7 XM_005248853.3:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X2 XM_006714997.3:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X3 XM_047418225.1:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X9 XM_047418227.1:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X5 XM_047418228.1:c. N/A Genic Downstream Transcript Variant
C6orf141 transcript variant X10 XM_047418231.1:c. N/A Genic Downstream Transcript Variant
Help

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
Help

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.p14 chr 6 NC_000006.12:g.49556579= NC_000006.12:g.49556579G>A
GRCh37.p13 chr 6 NC_000006.11:g.49524292= NC_000006.11:g.49524292G>A
C6orf141 transcript variant X4 XM_047418226.1:c.*3019+1422= XM_047418226.1:c.*3019+1422G>A
C6orf141 transcript variant X6 XM_047418229.1:c.*3124+1422= XM_047418229.1:c.*3124+1422G>A
C6orf141 transcript variant X8 XM_047418230.1:c.*666+1422= XM_047418230.1:c.*666+1422G>A
Help

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#.

2 SubSNP, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss4141552216 Apr 26, 2021 (155)
2 TOPMED ss4702606959 Apr 26, 2021 (155)
3 gnomAD - Genomes NC_000006.12 - 49556579 Apr 26, 2021 (155)
4 TopMed NC_000006.12 - 49556579 Apr 26, 2021 (155)
5 ALFA NC_000006.12 - 49556579 Apr 26, 2021 (155)
Help

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
224884956, 539984517, 11097304411, ss4141552216, ss4702606959 NC_000006.12:49556578:G:A NC_000006.12:49556578:G:A (self)
Help

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

No publications for rs1489537336

Help

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.post820+afb47a3d