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rs794728389

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728389(A;A)
Make rs794728389(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950176
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728389
ebirs794728389
HLIrs794728389
Exacrs794728389
Varsomers794728389
Maprs794728389
PheGenIrs794728389
hapmaprs794728389
1000 genomesrs794728389
hgdprs794728389
ensemblrs794728389
gopubmedrs794728389
geneviewrs794728389
scholarrs794728389
googlers794728389
pharmgkbrs794728389
gwascentralrs794728389
openSNPrs794728389
23andMers794728389
23andMe allrs794728389
SNP Nexus

SNPshotrs794728389
SNPdbers794728389
MSV3drs794728389
GWAS Ctlgrs794728389
Max Magnitude0
ClinVar
Risk rs794728389(A;A)
Alt rs794728389(A;A)
Reference rs794728389(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene KCNH2
CLNDBN not provided not specified
Reversed 1
HGVS NC_000007.13:g.150647264G>T
CLNSRC
CLNACC RCV000181856.1, RCV000223774.1,