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rs12632942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs12632942(A;G)
Make rs12632942(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38723507
GeneSCN10A
is asnp
is mentioned by
dbSNPrs12632942
dbSNP (classic)rs12632942
ClinGenrs12632942
ebirs12632942
HLIrs12632942
Exacrs12632942
Gnomadrs12632942
Varsomers12632942
LitVarrs12632942
Maprs12632942
PheGenIrs12632942
Biobankrs12632942
1000 genomesrs12632942
hgdprs12632942
ensemblrs12632942
geneviewrs12632942
scholarrs12632942
googlers12632942
pharmgkbrs12632942
gwascentralrs12632942
openSNPrs12632942
23andMers12632942
SNPshotrs12632942
SNPdbers12632942
MSV3drs12632942
GWAS Ctlgrs12632942
GMAF0.2378
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 24072447OA-icon.png] Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation


[PMID 20062060OA-icon.png] 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,