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rs199472963

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472963(A;G)
Make rs199472963(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951490
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472963
ebirs199472963
HLIrs199472963
Exacrs199472963
Varsomers199472963
Maprs199472963
PheGenIrs199472963
hapmaprs199472963
1000 genomesrs199472963
hgdprs199472963
ensemblrs199472963
gopubmedrs199472963
geneviewrs199472963
scholarrs199472963
googlers199472963
pharmgkbrs199472963
gwascentralrs199472963
openSNPrs199472963
23andMers199472963
23andMe allrs199472963
SNP Nexus

SNPshotrs199472963
SNPdbers199472963
MSV3drs199472963
GWAS Ctlgrs199472963
Max Magnitude0
ClinVar
Risk rs199472963(G;G)
Alt rs199472963(G;G)
Reference rs199472963(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648578T>C
CLNSRC ClinVar
CLNACC RCV000058045.2,