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rs794728417

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728417(A;T)
Make rs794728417(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974715
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728417
ebirs794728417
HLIrs794728417
Exacrs794728417
Varsomers794728417
Maprs794728417
PheGenIrs794728417
hapmaprs794728417
1000 genomesrs794728417
hgdprs794728417
ensemblrs794728417
gopubmedrs794728417
geneviewrs794728417
scholarrs794728417
googlers794728417
pharmgkbrs794728417
gwascentralrs794728417
openSNPrs794728417
23andMers794728417
23andMe allrs794728417
SNP Nexus

SNPshotrs794728417
SNPdbers794728417
MSV3drs794728417
GWAS Ctlgrs794728417
Max Magnitude0
ClinVar
Risk rs794728417(T;T)
Alt rs794728417(T;T)
Reference rs794728417(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671803T>A
CLNSRC
CLNACC RCV000181952.2,