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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.

rs192484924

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:231529417 (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=0.000200 (53/264690, TOPMED)
A=0.000128 (18/140234, GnomAD)
A=0.00021 (3/14050, ALFA) (+ 3 more)
A=0.0006 (4/6404, 1000G_30x)
A=0.0004 (2/5008, 1000G)
A=0.002 (1/534, MGP)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TSNAX : Intron Variant
TSNAX-DISC1 : Intron Variant
LOC122526782 : 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 14050 G=0.99979 A=0.00021
European Sub 9690 G=0.9997 A=0.0003
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


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=0.999800 A=0.000200
gnomAD - Genomes Global Study-wide 140234 G=0.999872 A=0.000128
gnomAD - Genomes European Sub 75952 G=0.99988 A=0.00012
gnomAD - Genomes African Sub 42018 G=0.99995 A=0.00005
gnomAD - Genomes American Sub 13660 G=0.99971 A=0.00029
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3130 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=0.9986 A=0.0014
Allele Frequency Aggregator Total Global 14050 G=0.99979 A=0.00021
Allele Frequency Aggregator European Sub 9690 G=0.9997 A=0.0003
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
1000Genomes_30x Global Study-wide 6404 G=0.9994 A=0.0006
1000Genomes_30x African Sub 1786 G=1.0000 A=0.0000
1000Genomes_30x Europe Sub 1266 G=1.0000 A=0.0000
1000Genomes_30x South Asian Sub 1202 G=1.0000 A=0.0000
1000Genomes_30x East Asian Sub 1170 G=1.0000 A=0.0000
1000Genomes_30x American Sub 980 G=0.996 A=0.004
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=1.0000 A=0.0000
1000Genomes Europe Sub 1006 G=1.0000 A=0.0000
1000Genomes South Asian Sub 978 G=1.000 A=0.000
1000Genomes American Sub 694 G=0.997 A=0.003
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.998 A=0.002
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 1 NC_000001.11:g.231529417G>A
GRCh37.p13 chr 1 NC_000001.10:g.231665163G>A
LOC126806044 genomic region NG_082368.1:g.1292G>A
Gene: TSNAX, translin associated factor X (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TSNAX transcript NM_005999.3:c.121+58G>A N/A Intron Variant
Gene: TSNAX-DISC1, TSNAX-DISC1 readthrough (NMD candidate) (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TSNAX-DISC1 transcript variant 1 NR_028393.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 2 NR_028394.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 3 NR_028395.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 4 NR_028396.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 5 NR_028397.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 6 NR_028398.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 7 NR_028399.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 8 NR_028400.1:n. N/A Intron Variant
Gene: LOC122526782, uncharacterized LOC122526782 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
LOC122526782 transcript NR_173106.1:n. N/A Upstream 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 1 NC_000001.11:g.231529417= NC_000001.11:g.231529417G>A
GRCh37.p13 chr 1 NC_000001.10:g.231665163= NC_000001.10:g.231665163G>A
LOC126806044 genomic region NG_082368.1:g.1292= NG_082368.1:g.1292G>A
TSNAX transcript NM_005999.2:c.121+58= NM_005999.2:c.121+58G>A
TSNAX transcript NM_005999.3:c.121+58= NM_005999.3:c.121+58G>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#.

14 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss454733190 Sep 17, 2011 (135)
2 CSHL ss472328930 May 04, 2012 (137)
3 1000GENOMES ss1295058470 Aug 21, 2014 (142)
4 EVA_MGP ss1710947699 Apr 01, 2015 (144)
5 CSHL ss2136844810 Nov 08, 2017 (151)
6 HUMAN_LONGEVITY ss2170928500 Dec 20, 2016 (150)
7 GNOMAD ss2767376026 Nov 08, 2017 (151)
8 TOPMED ss4487158385 Apr 25, 2021 (155)
9 1000G_HIGH_COVERAGE ss5246152335 Oct 13, 2022 (156)
10 EVA ss5325442046 Oct 13, 2022 (156)
11 HUGCELL_USP ss5446552763 Oct 13, 2022 (156)
12 1000G_HIGH_COVERAGE ss5520428988 Oct 13, 2022 (156)
13 EVA ss5912384774 Oct 13, 2022 (156)
14 EVA ss5939497296 Oct 13, 2022 (156)
15 1000Genomes NC_000001.10 - 231665163 Oct 11, 2018 (152)
16 1000Genomes_30x NC_000001.11 - 231529417 Oct 13, 2022 (156)
17 gnomAD - Genomes NC_000001.11 - 231529417 Apr 25, 2021 (155)
18 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 231665163 Apr 25, 2020 (154)
19 TopMed NC_000001.11 - 231529417 Apr 25, 2021 (155)
20 ALFA NC_000001.11 - 231529417 Apr 25, 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
ss2136844810 NC_000001.9:229731785:G:A NC_000001.11:231529416:G:A (self)
5927798, 64451, ss454733190, ss1295058470, ss1710947699, ss2767376026, ss5325442046, ss5939497296 NC_000001.10:231665162:G:A NC_000001.11:231529416:G:A (self)
7954923, 42527095, 50764720, 13283408696, ss2170928500, ss4487158385, ss5246152335, ss5446552763, ss5520428988, ss5912384774 NC_000001.11:231529416:G:A NC_000001.11:231529416:G:A (self)
ss472328930 NT_167186.1:25182941:G:A NC_000001.11:231529416: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 rs192484924

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.post761+d5e8e07