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rs796052195

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052195(C;C)
Make rs796052195(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951544
GeneKCNH2
is asnp
is mentioned by
dbSNPrs796052195
ebirs796052195
HLIrs796052195
Exacrs796052195
Varsomers796052195
Maprs796052195
PheGenIrs796052195
hapmaprs796052195
1000 genomesrs796052195
hgdprs796052195
ensemblrs796052195
gopubmedrs796052195
geneviewrs796052195
scholarrs796052195
googlers796052195
pharmgkbrs796052195
gwascentralrs796052195
openSNPrs796052195
23andMers796052195
23andMe allrs796052195
SNP Nexus

SNPshotrs796052195
SNPdbers796052195
MSV3drs796052195
GWAS Ctlgrs796052195
Max Magnitude0
ClinVar
Risk rs796052195(C;C)
Alt rs796052195(C;C)
Reference rs796052195(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648632A>G
CLNSRC
CLNACC RCV000190214.1,