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rs199472966

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472966(C;C)
Make rs199472966(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951482
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472966
ebirs199472966
HLIrs199472966
Exacrs199472966
Varsomers199472966
Maprs199472966
PheGenIrs199472966
hapmaprs199472966
1000 genomesrs199472966
hgdprs199472966
ensemblrs199472966
gopubmedrs199472966
geneviewrs199472966
scholarrs199472966
googlers199472966
pharmgkbrs199472966
gwascentralrs199472966
openSNPrs199472966
23andMers199472966
23andMe allrs199472966
SNP Nexus

SNPshotrs199472966
SNPdbers199472966
MSV3drs199472966
GWAS Ctlgrs199472966
Max Magnitude0
ClinVar
Risk rs199472966(C;C)
Alt rs199472966(C;C)
Reference rs199472966(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648570C>G
CLNSRC ClinVar
CLNACC RCV000058050.2,