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rs199473138

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473138(A;A)
Make rs199473138(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38598981
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473138
ebirs199473138
HLIrs199473138
Exacrs199473138
Varsomers199473138
Maprs199473138
PheGenIrs199473138
hapmaprs199473138
1000 genomesrs199473138
hgdprs199473138
ensemblrs199473138
gopubmedrs199473138
geneviewrs199473138
scholarrs199473138
googlers199473138
pharmgkbrs199473138
gwascentralrs199473138
openSNPrs199473138
23andMers199473138
23andMe allrs199473138
SNP Nexus

SNPshotrs199473138
SNPdbers199473138
MSV3drs199473138
GWAS Ctlgrs199473138
Max Magnitude0
ClinVar
Risk rs199473138(A;A)
Alt rs199473138(A;A)
Reference rs199473138(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38640472C>T
CLNSRC ClinVar
CLNACC RCV000058467.2,