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rs794728393

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728393(A;T)
Make rs794728393(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948954
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728393
ebirs794728393
HLIrs794728393
Exacrs794728393
Varsomers794728393
Maprs794728393
PheGenIrs794728393
hapmaprs794728393
1000 genomesrs794728393
hgdprs794728393
ensemblrs794728393
gopubmedrs794728393
geneviewrs794728393
scholarrs794728393
googlers794728393
pharmgkbrs794728393
gwascentralrs794728393
openSNPrs794728393
23andMers794728393
23andMe allrs794728393
SNP Nexus

SNPshotrs794728393
SNPdbers794728393
MSV3drs794728393
GWAS Ctlgrs794728393
Max Magnitude0
ClinVar
Risk rs794728393(T;T)
Alt rs794728393(T;T)
Reference rs794728393(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150646042T>A
CLNSRC
CLNACC RCV000181869.2,