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rs794728413

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728413(G;T)
Make rs794728413(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974743
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728413
ebirs794728413
HLIrs794728413
Exacrs794728413
Varsomers794728413
Maprs794728413
PheGenIrs794728413
hapmaprs794728413
1000 genomesrs794728413
hgdprs794728413
ensemblrs794728413
gopubmedrs794728413
geneviewrs794728413
scholarrs794728413
googlers794728413
pharmgkbrs794728413
gwascentralrs794728413
openSNPrs794728413
23andMers794728413
23andMe allrs794728413
SNP Nexus

SNPshotrs794728413
SNPdbers794728413
MSV3drs794728413
GWAS Ctlgrs794728413
Max Magnitude0
ClinVar
Risk rs794728413(T;T)
Alt rs794728413(T;T)
Reference rs794728413(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671831C>A
CLNSRC
CLNACC RCV000181943.2,