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rs794728394

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728394(A;T)
Make rs794728394(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947880
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728394
ebirs794728394
HLIrs794728394
Exacrs794728394
Varsomers794728394
Maprs794728394
PheGenIrs794728394
hapmaprs794728394
1000 genomesrs794728394
hgdprs794728394
ensemblrs794728394
gopubmedrs794728394
geneviewrs794728394
scholarrs794728394
googlers794728394
pharmgkbrs794728394
gwascentralrs794728394
openSNPrs794728394
23andMers794728394
23andMe allrs794728394
SNP Nexus

SNPshotrs794728394
SNPdbers794728394
MSV3drs794728394
GWAS Ctlgrs794728394
Max Magnitude0
ClinVar
Risk rs794728394(T;T)
Alt rs794728394(T;T)
Reference rs794728394(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644968T>A
CLNSRC
CLNACC RCV000181870.1,