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rs794728351

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728351(G;G)
Make rs794728351(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959700
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728351
ebirs794728351
HLIrs794728351
Exacrs794728351
Varsomers794728351
Maprs794728351
PheGenIrs794728351
hapmaprs794728351
1000 genomesrs794728351
hgdprs794728351
ensemblrs794728351
gopubmedrs794728351
geneviewrs794728351
scholarrs794728351
googlers794728351
pharmgkbrs794728351
gwascentralrs794728351
openSNPrs794728351
23andMers794728351
23andMe allrs794728351
SNP Nexus

SNPshotrs794728351
SNPdbers794728351
MSV3drs794728351
GWAS Ctlgrs794728351
Max Magnitude0
ClinVar
Risk rs794728351(G;G)
Alt rs794728351(G;G)
Reference rs794728351(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150656788A>C
CLNSRC
CLNACC RCV000181752.1,