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rs199473150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473150(C;T)
Make rs199473150(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38597799
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473150
ebirs199473150
HLIrs199473150
Exacrs199473150
Varsomers199473150
Maprs199473150
PheGenIrs199473150
hapmaprs199473150
1000 genomesrs199473150
hgdprs199473150
ensemblrs199473150
gopubmedrs199473150
geneviewrs199473150
scholarrs199473150
googlers199473150
pharmgkbrs199473150
gwascentralrs199473150
openSNPrs199473150
23andMers199473150
23andMe allrs199473150
SNP Nexus

SNPshotrs199473150
SNPdbers199473150
MSV3drs199473150
GWAS Ctlgrs199473150
Max Magnitude0
ClinVar
Risk rs199473150(T;T)
Alt rs199473150(T;T)
Reference rs199473150(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.38639290G>A
CLNSRC ClinVar
CLNACC RCV000058485.2,