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rs794728409

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728409(G;T)
Make rs794728409(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974879
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728409
ebirs794728409
HLIrs794728409
Exacrs794728409
Varsomers794728409
Maprs794728409
PheGenIrs794728409
hapmaprs794728409
1000 genomesrs794728409
hgdprs794728409
ensemblrs794728409
gopubmedrs794728409
geneviewrs794728409
scholarrs794728409
googlers794728409
pharmgkbrs794728409
gwascentralrs794728409
openSNPrs794728409
23andMers794728409
23andMe allrs794728409
SNP Nexus

SNPshotrs794728409
SNPdbers794728409
MSV3drs794728409
GWAS Ctlgrs794728409
Max Magnitude0
ClinVar
Risk rs794728409(T;T)
Alt rs794728409(T;T)
Reference rs794728409(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671967C>A
CLNSRC
CLNACC RCV000181929.2,