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

rs794728379

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728379(A;A)
Make rs794728379(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951477
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728379
ebirs794728379
HLIrs794728379
Exacrs794728379
Varsomers794728379
Maprs794728379
PheGenIrs794728379
hapmaprs794728379
1000 genomesrs794728379
hgdprs794728379
ensemblrs794728379
gopubmedrs794728379
geneviewrs794728379
scholarrs794728379
googlers794728379
pharmgkbrs794728379
gwascentralrs794728379
openSNPrs794728379
23andMers794728379
23andMe allrs794728379
SNP Nexus

SNPshotrs794728379
SNPdbers794728379
MSV3drs794728379
GWAS Ctlgrs794728379
Max Magnitude0
ClinVar
Risk rs794728379(A;A)
Alt rs794728379(A;A)
Reference rs794728379(T;T)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150648565A>T
CLNSRC
CLNACC RCV000181829.1,