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rs199472901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472901(C;T)
Make rs199472901(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952675
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472901
ebirs199472901
HLIrs199472901
Exacrs199472901
Varsomers199472901
Maprs199472901
PheGenIrs199472901
hapmaprs199472901
1000 genomesrs199472901
hgdprs199472901
ensemblrs199472901
gopubmedrs199472901
geneviewrs199472901
scholarrs199472901
googlers199472901
pharmgkbrs199472901
gwascentralrs199472901
openSNPrs199472901
23andMers199472901
23andMe allrs199472901
SNP Nexus

SNPshotrs199472901
SNPdbers199472901
MSV3drs199472901
GWAS Ctlgrs199472901
Max Magnitude0
ClinVar
Risk rs199472901(T;T)
Alt rs199472901(T;T)
Reference rs199472901(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649763G>A
CLNSRC ClinVar
CLNACC RCV000057891.2,