Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473077(A;A)
Make rs199473077(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609935
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473077
ebirs199473077
HLIrs199473077
Exacrs199473077
Varsomers199473077
Maprs199473077
PheGenIrs199473077
hapmaprs199473077
1000 genomesrs199473077
hgdprs199473077
ensemblrs199473077
gopubmedrs199473077
geneviewrs199473077
scholarrs199473077
googlers199473077
pharmgkbrs199473077
gwascentralrs199473077
openSNPrs199473077
23andMers199473077
23andMe allrs199473077
SNP Nexus

SNPshotrs199473077
SNPdbers199473077
MSV3drs199473077
GWAS Ctlgrs199473077
Max Magnitude0
ClinVar
Risk rs199473077(A;A)
Alt rs199473077(A;A)
Reference rs199473077(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38651426G>T
CLNSRC ClinVar
CLNACC RCV000058843.2,