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rs794728369

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728369(C;C)
Make rs794728369(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952567
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728369
ebirs794728369
HLIrs794728369
Exacrs794728369
Varsomers794728369
Maprs794728369
PheGenIrs794728369
hapmaprs794728369
1000 genomesrs794728369
hgdprs794728369
ensemblrs794728369
gopubmedrs794728369
geneviewrs794728369
scholarrs794728369
googlers794728369
pharmgkbrs794728369
gwascentralrs794728369
openSNPrs794728369
23andMers794728369
23andMe allrs794728369
SNP Nexus

SNPshotrs794728369
SNPdbers794728369
MSV3drs794728369
GWAS Ctlgrs794728369
Max Magnitude0
ClinVar
Risk rs794728369(C;C)
Alt rs794728369(C;C)
Reference rs794728369(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649655C>G
CLNSRC
CLNACC RCV000181790.1,