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rs794728494

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728494(C;C)
Make rs794728494(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position150974783
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728494
ebirs794728494
HLIrs794728494
Exacrs794728494
Varsomers794728494
Maprs794728494
PheGenIrs794728494
hapmaprs794728494
1000 genomesrs794728494
hgdprs794728494
ensemblrs794728494
gopubmedrs794728494
geneviewrs794728494
scholarrs794728494
googlers794728494
pharmgkbrs794728494
gwascentralrs794728494
openSNPrs794728494
23andMers794728494
23andMe allrs794728494
SNP Nexus

SNPshotrs794728494
SNPdbers794728494
MSV3drs794728494
GWAS Ctlgrs794728494
Max Magnitude0
ClinVar
Risk rs794728494(C;C)
Alt rs794728494(C;C)
Reference rs794728494(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671871C>G
CLNSRC
CLNACC RCV000182052.2,