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rs199473035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473035(C;T)
Make rs199473035(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150945388
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473035
ebirs199473035
HLIrs199473035
Exacrs199473035
Varsomers199473035
Maprs199473035
PheGenIrs199473035
hapmaprs199473035
1000 genomesrs199473035
hgdprs199473035
ensemblrs199473035
gopubmedrs199473035
geneviewrs199473035
scholarrs199473035
googlers199473035
pharmgkbrs199473035
gwascentralrs199473035
openSNPrs199473035
23andMers199473035
23andMe allrs199473035
SNP Nexus

SNPshotrs199473035
SNPdbers199473035
MSV3drs199473035
GWAS Ctlgrs199473035
Max Magnitude0
ClinVar
Risk rs199473035(T;T)
Alt rs199473035(T;T)
Reference rs199473035(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.150642476G>A
CLNSRC ClinVar
CLNACC RCV000058226.2,