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rs794728462

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728462(-;C)
Make rs794728462(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947678
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728462
ClinGenrs794728462
ebirs794728462
HLIrs794728462
Exacrs794728462
Varsomers794728462
Maprs794728462
PheGenIrs794728462
hapmaprs794728462
1000 genomesrs794728462
hgdprs794728462
ensemblrs794728462
gopubmedrs794728462
geneviewrs794728462
scholarrs794728462
googlers794728462
pharmgkbrs794728462
gwascentralrs794728462
openSNPrs794728462
23andMers794728462
23andMe allrs794728462
SNP Nexus

SNPshotrs794728462
SNPdbers794728462
MSV3drs794728462
GWAS Ctlgrs794728462
Max Magnitude0
ClinVar
Risk rs794728462(C;C)
Alt rs794728462(C;C)
Reference Rs794728462(;)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644767dupG
CLNSRC
CLNACC RCV000182000.1,