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

rs794728374

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728374(C;T)
Make rs794728374(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951718
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728374
ebirs794728374
HLIrs794728374
Exacrs794728374
Varsomers794728374
Maprs794728374
PheGenIrs794728374
hapmaprs794728374
1000 genomesrs794728374
hgdprs794728374
ensemblrs794728374
gopubmedrs794728374
geneviewrs794728374
scholarrs794728374
googlers794728374
pharmgkbrs794728374
gwascentralrs794728374
openSNPrs794728374
23andMers794728374
23andMe allrs794728374
SNP Nexus

SNPshotrs794728374
SNPdbers794728374
MSV3drs794728374
GWAS Ctlgrs794728374
Max Magnitude0
ClinVar
Risk rs794728374(T;T)
Alt rs794728374(T;T)
Reference rs794728374(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648806G>A
CLNSRC
CLNACC RCV000181804.1,