Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728386

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728386(A;A)
Make rs794728386(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950303
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728386
ebirs794728386
HLIrs794728386
Exacrs794728386
Varsomers794728386
Maprs794728386
PheGenIrs794728386
hapmaprs794728386
1000 genomesrs794728386
hgdprs794728386
ensemblrs794728386
gopubmedrs794728386
geneviewrs794728386
scholarrs794728386
googlers794728386
pharmgkbrs794728386
gwascentralrs794728386
openSNPrs794728386
23andMers794728386
23andMe allrs794728386
SNP Nexus

SNPshotrs794728386
SNPdbers794728386
MSV3drs794728386
GWAS Ctlgrs794728386
Max Magnitude0
ClinVar
Risk rs794728386(A;A)
Alt rs794728386(A;A)
Reference rs794728386(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647391C>T
CLNSRC
CLNACC RCV000181846.1,