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rs794728350

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728350(C;G)
Make rs794728350(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959703
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728350
ebirs794728350
HLIrs794728350
Exacrs794728350
Varsomers794728350
Maprs794728350
PheGenIrs794728350
hapmaprs794728350
1000 genomesrs794728350
hgdprs794728350
ensemblrs794728350
gopubmedrs794728350
geneviewrs794728350
scholarrs794728350
googlers794728350
pharmgkbrs794728350
gwascentralrs794728350
openSNPrs794728350
23andMers794728350
23andMe allrs794728350
SNP Nexus

SNPshotrs794728350
SNPdbers794728350
MSV3drs794728350
GWAS Ctlgrs794728350
Max Magnitude0
ClinVar
Risk rs794728350(G;G)
Alt rs794728350(G;G)
Reference rs794728350(C;C)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150656791G>C
CLNSRC
CLNACC RCV000181751.1,