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rs794728402

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728402(G;T)
Make rs794728402(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947473
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728402
ebirs794728402
HLIrs794728402
Exacrs794728402
Varsomers794728402
Maprs794728402
PheGenIrs794728402
hapmaprs794728402
1000 genomesrs794728402
hgdprs794728402
ensemblrs794728402
gopubmedrs794728402
geneviewrs794728402
scholarrs794728402
googlers794728402
pharmgkbrs794728402
gwascentralrs794728402
openSNPrs794728402
23andMers794728402
23andMe allrs794728402
SNP Nexus

SNPshotrs794728402
SNPdbers794728402
MSV3drs794728402
GWAS Ctlgrs794728402
Max Magnitude0
ClinVar
Risk rs794728402(T;T)
Alt rs794728402(T;T)
Reference rs794728402(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644561C>A
CLNSRC
CLNACC RCV000181906.1,