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rs794728373

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728373(A;A)
Make rs794728373(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951783
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728373
ebirs794728373
HLIrs794728373
Exacrs794728373
Varsomers794728373
Maprs794728373
PheGenIrs794728373
hapmaprs794728373
1000 genomesrs794728373
hgdprs794728373
ensemblrs794728373
gopubmedrs794728373
geneviewrs794728373
scholarrs794728373
googlers794728373
pharmgkbrs794728373
gwascentralrs794728373
openSNPrs794728373
23andMers794728373
23andMe allrs794728373
SNP Nexus

SNPshotrs794728373
SNPdbers794728373
MSV3drs794728373
GWAS Ctlgrs794728373
Max Magnitude0
ClinVar
Risk rs794728373(A;A)
Alt rs794728373(A;A)
Reference rs794728373(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648871C>T
CLNSRC
CLNACC RCV000181802.2,