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

rs794728477

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728477(C;C)
Make rs794728477(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959571
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728477
ebirs794728477
HLIrs794728477
Exacrs794728477
Varsomers794728477
Maprs794728477
PheGenIrs794728477
hapmaprs794728477
1000 genomesrs794728477
hgdprs794728477
ensemblrs794728477
gopubmedrs794728477
geneviewrs794728477
scholarrs794728477
googlers794728477
pharmgkbrs794728477
gwascentralrs794728477
openSNPrs794728477
23andMers794728477
23andMe allrs794728477
SNP Nexus

SNPshotrs794728477
SNPdbers794728477
MSV3drs794728477
GWAS Ctlgrs794728477
Max Magnitude0
ClinVar
Risk rs794728477(C;C)
Alt rs794728477(C;C)
Reference rs794728477(G;G)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150656659C>G
CLNSRC
CLNACC RCV000182017.1,