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rs199473038

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473038(G;G)
Make rs199473038(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951697
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473038
ebirs199473038
HLIrs199473038
Exacrs199473038
Varsomers199473038
Maprs199473038
PheGenIrs199473038
hapmaprs199473038
1000 genomesrs199473038
hgdprs199473038
ensemblrs199473038
gopubmedrs199473038
geneviewrs199473038
scholarrs199473038
googlers199473038
pharmgkbrs199473038
gwascentralrs199473038
openSNPrs199473038
23andMers199473038
23andMe allrs199473038
SNP Nexus

SNPshotrs199473038
SNPdbers199473038
MSV3drs199473038
GWAS Ctlgrs199473038
Max Magnitude0
ClinVar
Risk rs199473038(G;G)
Alt rs199473038(G;G)
Reference rs199473038(T;T)
Significance Probable-Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648785A>C
CLNSRC ClinVar
CLNACC RCV000057948.2,