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rs794728461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728461(-;A)
Make rs794728461(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947773
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728461
ClinGenrs794728461
ebirs794728461
HLIrs794728461
Exacrs794728461
Varsomers794728461
Maprs794728461
PheGenIrs794728461
hapmaprs794728461
1000 genomesrs794728461
hgdprs794728461
ensemblrs794728461
gopubmedrs794728461
geneviewrs794728461
scholarrs794728461
googlers794728461
pharmgkbrs794728461
gwascentralrs794728461
openSNPrs794728461
23andMers794728461
23andMe allrs794728461
SNP Nexus

SNPshotrs794728461
SNPdbers794728461
MSV3drs794728461
GWAS Ctlgrs794728461
Max Magnitude0
ClinVar
Risk rs794728461(A;A)
Alt rs794728461(A;A)
Reference Rs794728461(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644862dupT
CLNSRC
CLNACC RCV000181999.1,