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rs794729111

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729111(G;G)
Make rs794729111(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32822606
GenePKP2
is asnp
is mentioned by
dbSNPrs794729111
ebirs794729111
HLIrs794729111
Exacrs794729111
Varsomers794729111
Maprs794729111
PheGenIrs794729111
hapmaprs794729111
1000 genomesrs794729111
hgdprs794729111
ensemblrs794729111
gopubmedrs794729111
geneviewrs794729111
scholarrs794729111
googlers794729111
pharmgkbrs794729111
gwascentralrs794729111
openSNPrs794729111
23andMers794729111
23andMe allrs794729111
SNP Nexus

SNPshotrs794729111
SNPdbers794729111
MSV3drs794729111
GWAS Ctlgrs794729111
Max Magnitude0
ClinVar
Risk rs794729111(G;G)
Alt rs794729111(G;G)
Reference rs794729111(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32975540A>C
CLNSRC
CLNACC RCV000183758.1,