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rs794728384

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728384(A;A)
Make rs794728384(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950921
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728384
ebirs794728384
HLIrs794728384
Exacrs794728384
Varsomers794728384
Maprs794728384
PheGenIrs794728384
hapmaprs794728384
1000 genomesrs794728384
hgdprs794728384
ensemblrs794728384
gopubmedrs794728384
geneviewrs794728384
scholarrs794728384
googlers794728384
pharmgkbrs794728384
gwascentralrs794728384
openSNPrs794728384
23andMers794728384
23andMe allrs794728384
SNP Nexus

SNPshotrs794728384
SNPdbers794728384
MSV3drs794728384
GWAS Ctlgrs794728384
Max Magnitude0
ClinVar
Risk rs794728384(A;A)
Alt rs794728384(A;A)
Reference rs794728384(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648009C>T
CLNSRC
CLNACC RCV000181840.2,