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rs794728383

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728383(A;A)
Make rs794728383(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950985
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728383
ebirs794728383
HLIrs794728383
Exacrs794728383
Varsomers794728383
Maprs794728383
PheGenIrs794728383
hapmaprs794728383
1000 genomesrs794728383
hgdprs794728383
ensemblrs794728383
gopubmedrs794728383
geneviewrs794728383
scholarrs794728383
googlers794728383
pharmgkbrs794728383
gwascentralrs794728383
openSNPrs794728383
23andMers794728383
23andMe allrs794728383
SNP Nexus

SNPshotrs794728383
SNPdbers794728383
MSV3drs794728383
GWAS Ctlgrs794728383
Max Magnitude0
ClinVar
Risk rs794728383(A;A)
Alt rs794728383(A;A)
Reference rs794728383(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648073C>T
CLNSRC
CLNACC RCV000181837.2,