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rs794728372

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728372(C;T)
Make rs794728372(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952462
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728372
ebirs794728372
HLIrs794728372
Exacrs794728372
Varsomers794728372
Maprs794728372
PheGenIrs794728372
hapmaprs794728372
1000 genomesrs794728372
hgdprs794728372
ensemblrs794728372
gopubmedrs794728372
geneviewrs794728372
scholarrs794728372
googlers794728372
pharmgkbrs794728372
gwascentralrs794728372
openSNPrs794728372
23andMers794728372
23andMe allrs794728372
SNP Nexus

SNPshotrs794728372
SNPdbers794728372
MSV3drs794728372
GWAS Ctlgrs794728372
Max Magnitude0
ClinVar
Risk rs794728372(T;T)
Alt rs794728372(T;T)
Reference rs794728372(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.150649550G>A
CLNSRC
CLNACC RCV000181797.2,