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rs199473181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473181(G;T)
Make rs199473181(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581265
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473181
ebirs199473181
HLIrs199473181
Exacrs199473181
Varsomers199473181
Maprs199473181
PheGenIrs199473181
hapmaprs199473181
1000 genomesrs199473181
hgdprs199473181
ensemblrs199473181
gopubmedrs199473181
geneviewrs199473181
scholarrs199473181
googlers199473181
pharmgkbrs199473181
gwascentralrs199473181
openSNPrs199473181
23andMers199473181
23andMe allrs199473181
SNP Nexus

SNPshotrs199473181
SNPdbers199473181
MSV3drs199473181
GWAS Ctlgrs199473181
Max Magnitude0
ClinVar
Risk rs199473181(A,T;A,T)
Alt rs199473181(A,T;A,T)
Reference rs199473181(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38622756C>A; NC_000003.11:g.38622756C>T
CLNSRC ClinVar
CLNACC RCV000058535.2, RCV000058534.2,