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rs794728391

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728391(C;C)
Make rs794728391(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950167
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728391
ebirs794728391
HLIrs794728391
Exacrs794728391
Varsomers794728391
Maprs794728391
PheGenIrs794728391
hapmaprs794728391
1000 genomesrs794728391
hgdprs794728391
ensemblrs794728391
gopubmedrs794728391
geneviewrs794728391
scholarrs794728391
googlers794728391
pharmgkbrs794728391
gwascentralrs794728391
openSNPrs794728391
23andMers794728391
23andMe allrs794728391
SNP Nexus

SNPshotrs794728391
SNPdbers794728391
MSV3drs794728391
GWAS Ctlgrs794728391
Max Magnitude0
ClinVar
Risk rs794728391(C;C)
Alt rs794728391(C;C)
Reference rs794728391(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647255C>G
CLNSRC
CLNACC RCV000181858.2,