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rs199472886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472886(C;T)
Make rs199472886(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150957460
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472886
ebirs199472886
HLIrs199472886
Exacrs199472886
Varsomers199472886
Maprs199472886
PheGenIrs199472886
hapmaprs199472886
1000 genomesrs199472886
hgdprs199472886
ensemblrs199472886
gopubmedrs199472886
geneviewrs199472886
scholarrs199472886
googlers199472886
pharmgkbrs199472886
gwascentralrs199472886
openSNPrs199472886
23andMers199472886
23andMe allrs199472886
SNP Nexus

SNPshotrs199472886
SNPdbers199472886
MSV3drs199472886
GWAS Ctlgrs199472886
Max Magnitude0
ClinVar
Risk rs199472886(G,T;G,T)
Alt rs199472886(G,T;G,T)
Reference rs199472886(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150654548G>A; NC_000007.13:g.150654548G>C
CLNSRC ClinVar
CLNACC RCV000058279.2, RCV000181773.1,