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rs199472977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472977(G;G)
Make rs199472977(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951099
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472977
ebirs199472977
HLIrs199472977
Exacrs199472977
Varsomers199472977
Maprs199472977
PheGenIrs199472977
hapmaprs199472977
1000 genomesrs199472977
hgdprs199472977
ensemblrs199472977
gopubmedrs199472977
geneviewrs199472977
scholarrs199472977
googlers199472977
pharmgkbrs199472977
gwascentralrs199472977
openSNPrs199472977
23andMers199472977
23andMe allrs199472977
SNP Nexus

SNPshotrs199472977
SNPdbers199472977
MSV3drs199472977
GWAS Ctlgrs199472977
Max Magnitude0
ClinVar
Risk rs199472977(G;G)
Alt rs199472977(G;G)
Reference rs199472977(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648187A>C
CLNSRC ClinVar
CLNACC RCV000058067.2,