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rs794729133

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729133(A;G)
Make rs794729133(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32850975
GenePKP2
is asnp
is mentioned by
dbSNPrs794729133
ebirs794729133
HLIrs794729133
Exacrs794729133
Varsomers794729133
Maprs794729133
PheGenIrs794729133
hapmaprs794729133
1000 genomesrs794729133
hgdprs794729133
ensemblrs794729133
gopubmedrs794729133
geneviewrs794729133
scholarrs794729133
googlers794729133
pharmgkbrs794729133
gwascentralrs794729133
openSNPrs794729133
23andMers794729133
23andMe allrs794729133
SNP Nexus

SNPshotrs794729133
SNPdbers794729133
MSV3drs794729133
GWAS Ctlgrs794729133
Max Magnitude0
ClinVar
Risk rs794729133(G;G)
Alt rs794729133(G;G)
Reference rs794729133(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33003909T>C
CLNSRC
CLNACC RCV000183805.2,