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rs794728382

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728382(C;T)
Make rs794728382(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950962
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728382
ebirs794728382
HLIrs794728382
Exacrs794728382
Varsomers794728382
Maprs794728382
PheGenIrs794728382
hapmaprs794728382
1000 genomesrs794728382
hgdprs794728382
ensemblrs794728382
gopubmedrs794728382
geneviewrs794728382
scholarrs794728382
googlers794728382
pharmgkbrs794728382
gwascentralrs794728382
openSNPrs794728382
23andMers794728382
23andMe allrs794728382
SNP Nexus

SNPshotrs794728382
SNPdbers794728382
MSV3drs794728382
GWAS Ctlgrs794728382
Max Magnitude0
ClinVar
Risk rs794728382(T;T)
Alt rs794728382(T;T)
Reference rs794728382(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648050G>A
CLNSRC
CLNACC RCV000181835.1,