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rs199473641

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473641(A;G)
Make rs199473641(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581061
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473641
ebirs199473641
HLIrs199473641
Exacrs199473641
Varsomers199473641
Maprs199473641
PheGenIrs199473641
hapmaprs199473641
1000 genomesrs199473641
hgdprs199473641
ensemblrs199473641
gopubmedrs199473641
geneviewrs199473641
scholarrs199473641
googlers199473641
pharmgkbrs199473641
gwascentralrs199473641
openSNPrs199473641
23andMers199473641
23andMe allrs199473641
SNP Nexus

SNPshotrs199473641
SNPdbers199473641
MSV3drs199473641
GWAS Ctlgrs199473641
Max Magnitude0
ClinVar
Risk rs199473641(G;G)
Alt rs199473641(G;G)
Reference rs199473641(A;A)
Significance Probable-Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38622552T>C
CLNSRC ClinVar
CLNACC RCV000058547.2,