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rs199472961

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472961(A;G)
Make rs199472961(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951495
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472961
ebirs199472961
HLIrs199472961
Exacrs199472961
Varsomers199472961
Maprs199472961
PheGenIrs199472961
hapmaprs199472961
1000 genomesrs199472961
hgdprs199472961
ensemblrs199472961
gopubmedrs199472961
geneviewrs199472961
scholarrs199472961
googlers199472961
pharmgkbrs199472961
gwascentralrs199472961
openSNPrs199472961
23andMers199472961
23andMe allrs199472961
SNP Nexus

SNPshotrs199472961
SNPdbers199472961
MSV3drs199472961
GWAS Ctlgrs199472961
Max Magnitude0
ClinVar
Risk rs199472961(G,T;G,T)
Alt rs199472961(G,T;G,T)
Reference rs199472961(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150648583T>A; NC_000007.13:g.150648583T>C
CLNSRC ClinVar
CLNACC RCV000058043.2, RCV000058042.2, RCV000181825.2,