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rs794728387

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728387(A;A)
Make rs794728387(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950206
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728387
ebirs794728387
HLIrs794728387
Exacrs794728387
Varsomers794728387
Maprs794728387
PheGenIrs794728387
hapmaprs794728387
1000 genomesrs794728387
hgdprs794728387
ensemblrs794728387
gopubmedrs794728387
geneviewrs794728387
scholarrs794728387
googlers794728387
pharmgkbrs794728387
gwascentralrs794728387
openSNPrs794728387
23andMers794728387
23andMe allrs794728387
SNP Nexus

SNPshotrs794728387
SNPdbers794728387
MSV3drs794728387
GWAS Ctlgrs794728387
Max Magnitude0
ClinVar
Risk rs794728387(A;A)
Alt rs794728387(A;A)
Reference rs794728387(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647294A>T
CLNSRC
CLNACC RCV000181849.2,