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

rs794728399

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728399(A;A)
Make rs794728399(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947791
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728399
ebirs794728399
HLIrs794728399
Exacrs794728399
Varsomers794728399
Maprs794728399
PheGenIrs794728399
hapmaprs794728399
1000 genomesrs794728399
hgdprs794728399
ensemblrs794728399
gopubmedrs794728399
geneviewrs794728399
scholarrs794728399
googlers794728399
pharmgkbrs794728399
gwascentralrs794728399
openSNPrs794728399
23andMers794728399
23andMe allrs794728399
SNP Nexus

SNPshotrs794728399
SNPdbers794728399
MSV3drs794728399
GWAS Ctlgrs794728399
Max Magnitude0
ClinVar
Risk rs794728399(A,T;A,T)
Alt rs794728399(A,T;A,T)
Reference rs794728399(G;G)
Significance Pathogenic
Disease not specified Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN not specified Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644879C>A; NC_000007.13:g.150644879C>T
CLNSRC
CLNACC RCV000181895.2, RCV000181894.1,