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rs199472925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472925(G;T)
Make rs199472925(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951696
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472925
ebirs199472925
HLIrs199472925
Exacrs199472925
Varsomers199472925
Maprs199472925
PheGenIrs199472925
hapmaprs199472925
1000 genomesrs199472925
hgdprs199472925
ensemblrs199472925
gopubmedrs199472925
geneviewrs199472925
scholarrs199472925
googlers199472925
pharmgkbrs199472925
gwascentralrs199472925
openSNPrs199472925
23andMers199472925
23andMe allrs199472925
SNP Nexus

SNPshotrs199472925
SNPdbers199472925
MSV3drs199472925
GWAS Ctlgrs199472925
Max Magnitude0
ClinVar
Risk rs199472925(C,T;C,T)
Alt rs199472925(C,T;C,T)
Reference rs199472925(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.150648784C>A; NC_000007.13:g.150648784C>G
CLNSRC ClinVar
CLNACC RCV000057950.2, RCV000057949.2,