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rs794728487

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728487(A;A)
Make rs794728487(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951447
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728487
ebirs794728487
HLIrs794728487
Exacrs794728487
Varsomers794728487
Maprs794728487
PheGenIrs794728487
hapmaprs794728487
1000 genomesrs794728487
hgdprs794728487
ensemblrs794728487
gopubmedrs794728487
geneviewrs794728487
scholarrs794728487
googlers794728487
pharmgkbrs794728487
gwascentralrs794728487
openSNPrs794728487
23andMers794728487
23andMe allrs794728487
SNP Nexus

SNPshotrs794728487
SNPdbers794728487
MSV3drs794728487
GWAS Ctlgrs794728487
Max Magnitude0
ClinVar
Risk rs794728487(A;A)
Alt rs794728487(A;A)
Reference rs794728487(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648535C>T
CLNSRC
CLNACC RCV000182038.1,