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rs199472937

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472937(A;A)
Make rs199472937(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951582
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472937
ebirs199472937
HLIrs199472937
Exacrs199472937
Varsomers199472937
Maprs199472937
PheGenIrs199472937
hapmaprs199472937
1000 genomesrs199472937
hgdprs199472937
ensemblrs199472937
gopubmedrs199472937
geneviewrs199472937
scholarrs199472937
googlers199472937
pharmgkbrs199472937
gwascentralrs199472937
openSNPrs199472937
23andMers199472937
23andMe allrs199472937
SNP Nexus

SNPshotrs199472937
SNPdbers199472937
MSV3drs199472937
GWAS Ctlgrs199472937
Max Magnitude0
ClinVar
Risk rs199472937(A,T;A,T)
Alt rs199472937(A,T;A,T)
Reference rs199472937(G;G)
Significance Pathogenic
Disease not specified Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN not specified Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648670C>A; NC_000007.13:g.150648670C>T
CLNSRC ClinVar
CLNACC RCV000182030.1, RCV000057998.2,