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rs199473112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473112(C;G)
Make rs199473112(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38605956
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473112
ebirs199473112
HLIrs199473112
Exacrs199473112
Varsomers199473112
Maprs199473112
PheGenIrs199473112
hapmaprs199473112
1000 genomesrs199473112
hgdprs199473112
ensemblrs199473112
gopubmedrs199473112
geneviewrs199473112
scholarrs199473112
googlers199473112
pharmgkbrs199473112
gwascentralrs199473112
openSNPrs199473112
23andMers199473112
23andMe allrs199473112
SNP Nexus

SNPshotrs199473112
SNPdbers199473112
MSV3drs199473112
GWAS Ctlgrs199473112
Max Magnitude0
ClinVar
Risk rs199473112(G;G)
Alt rs199473112(G;G)
Reference rs199473112(C;C)
Significance Pathogenic
Disease Atrial fibrillation Atrial fibrillation
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation, familial, 10 Atrial fibrillation
Reversed 1
HGVS NC_000003.11:g.38647447G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022948.2, RCV000058414.2,


[PMID 18378609OA-icon.png] Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.