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rs199473422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473422(C;T)
Make rs199473422(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974797
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473422
ebirs199473422
HLIrs199473422
Exacrs199473422
Varsomers199473422
Maprs199473422
PheGenIrs199473422
hapmaprs199473422
1000 genomesrs199473422
hgdprs199473422
ensemblrs199473422
gopubmedrs199473422
geneviewrs199473422
scholarrs199473422
googlers199473422
pharmgkbrs199473422
gwascentralrs199473422
openSNPrs199473422
23andMers199473422
23andMe allrs199473422
SNP Nexus

SNPshotrs199473422
SNPdbers199473422
MSV3drs199473422
GWAS Ctlgrs199473422
Max Magnitude0
ClinVar
Risk rs199473422(G,T;G,T)
Alt rs199473422(G,T;G,T)
Reference rs199473422(C;C)
Significance Other
Disease not provided Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN not provided Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671885G>A; NC_000007.13:g.150671885G>C
CLNSRC ClinVar
CLNACC RCV000058097.3, RCV000058096.2, RCV000182051.1,