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rs794728410

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728410(C;G)
Make rs794728410(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974871
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728410
ebirs794728410
HLIrs794728410
Exacrs794728410
Varsomers794728410
Maprs794728410
PheGenIrs794728410
hapmaprs794728410
1000 genomesrs794728410
hgdprs794728410
ensemblrs794728410
gopubmedrs794728410
geneviewrs794728410
scholarrs794728410
googlers794728410
pharmgkbrs794728410
gwascentralrs794728410
openSNPrs794728410
23andMers794728410
23andMe allrs794728410
SNP Nexus

SNPshotrs794728410
SNPdbers794728410
MSV3drs794728410
GWAS Ctlgrs794728410
Max Magnitude0
ClinVar
Risk rs794728410(G;G)
Alt rs794728410(G;G)
Reference rs794728410(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671959G>C
CLNSRC
CLNACC RCV000181930.2,