rs12632942
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs12632942(A;G) |
Make rs12632942(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 38723507 |
Gene | SCN10A |
is a | snp |
is | mentioned by |
dbSNP | rs12632942 |
dbSNP (classic) | rs12632942 |
ClinGen | rs12632942 |
ebi | rs12632942 |
HLI | rs12632942 |
Exac | rs12632942 |
Gnomad | rs12632942 |
Varsome | rs12632942 |
LitVar | rs12632942 |
Map | rs12632942 |
PheGenI | rs12632942 |
Biobank | rs12632942 |
1000 genomes | rs12632942 |
hgdp | rs12632942 |
ensembl | rs12632942 |
geneview | rs12632942 |
scholar | rs12632942 |
rs12632942 | |
pharmgkb | rs12632942 |
gwascentral | rs12632942 |
openSNP | rs12632942 |
23andMe | rs12632942 |
SNPshot | rs12632942 |
SNPdbe | rs12632942 |
MSV3d | rs12632942 |
GWAS Ctlg | rs12632942 |
GMAF | 0.2378 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24072447] Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation
[PMID 20062060] Genome-wide association study of PR interval.
[PMID 23821303] Voltage-gated sodium channel polymorphisms play a pivotal role in the development of oxaliplatin-induced peripheral neurotoxicity: results from a prospective multicenter study.
ClinVar | |
---|---|
Risk | rs12632942(G;G) |
Alt | rs12632942(G;G) |
Reference | Rs12632942(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SCN10A |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.38764998A>G |
CLNSRC | |
CLNACC | RCV000253983.2, |