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rs794728493

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728493(C;T)
Make rs794728493(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974848
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728493
ebirs794728493
HLIrs794728493
Exacrs794728493
Varsomers794728493
Maprs794728493
PheGenIrs794728493
hapmaprs794728493
1000 genomesrs794728493
hgdprs794728493
ensemblrs794728493
gopubmedrs794728493
geneviewrs794728493
scholarrs794728493
googlers794728493
pharmgkbrs794728493
gwascentralrs794728493
openSNPrs794728493
23andMers794728493
23andMe allrs794728493
SNP Nexus

SNPshotrs794728493
SNPdbers794728493
MSV3drs794728493
GWAS Ctlgrs794728493
Max Magnitude0
ClinVar
Risk rs794728493(T;T)
Alt rs794728493(T;T)
Reference rs794728493(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671936G>A
CLNSRC
CLNACC RCV000182050.1,