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rs794728367

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728367(A;A)
Make rs794728367(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952756
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728367
ebirs794728367
HLIrs794728367
Exacrs794728367
Varsomers794728367
Maprs794728367
PheGenIrs794728367
hapmaprs794728367
1000 genomesrs794728367
hgdprs794728367
ensemblrs794728367
gopubmedrs794728367
geneviewrs794728367
scholarrs794728367
googlers794728367
pharmgkbrs794728367
gwascentralrs794728367
openSNPrs794728367
23andMers794728367
23andMe allrs794728367
SNP Nexus

SNPshotrs794728367
SNPdbers794728367
MSV3drs794728367
GWAS Ctlgrs794728367
Max Magnitude0
ClinVar
Risk rs794728367(A;A)
Alt rs794728367(A;A)
Reference rs794728367(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.150649844A>T
CLNSRC
CLNACC RCV000181783.2,