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rs794728419

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728419(G;G)
Make rs794728419(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150977836
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728419
ebirs794728419
HLIrs794728419
Exacrs794728419
Varsomers794728419
Maprs794728419
PheGenIrs794728419
hapmaprs794728419
1000 genomesrs794728419
hgdprs794728419
ensemblrs794728419
gopubmedrs794728419
geneviewrs794728419
scholarrs794728419
googlers794728419
pharmgkbrs794728419
gwascentralrs794728419
openSNPrs794728419
23andMers794728419
23andMe allrs794728419
SNP Nexus

SNPshotrs794728419
SNPdbers794728419
MSV3drs794728419
GWAS Ctlgrs794728419
Max Magnitude0
ClinVar
Risk rs794728419(G;G)
Alt rs794728419(G;G)
Reference rs794728419(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150674924A>C
CLNSRC
CLNACC RCV000181955.1,