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rs794728388

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728388(C;C)
Make rs794728388(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950200
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728388
ebirs794728388
HLIrs794728388
Exacrs794728388
Varsomers794728388
Maprs794728388
PheGenIrs794728388
hapmaprs794728388
1000 genomesrs794728388
hgdprs794728388
ensemblrs794728388
gopubmedrs794728388
geneviewrs794728388
scholarrs794728388
googlers794728388
pharmgkbrs794728388
gwascentralrs794728388
openSNPrs794728388
23andMers794728388
23andMe allrs794728388
SNP Nexus

SNPshotrs794728388
SNPdbers794728388
MSV3drs794728388
GWAS Ctlgrs794728388
Max Magnitude0
ClinVar
Risk rs794728388(C;C)
Alt rs794728388(C;C)
Reference rs794728388(T;T)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150647288A>G
CLNSRC
CLNACC RCV000181851.1,