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rs794729108

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729108(G;G)
Make rs794729108(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32824084
GenePKP2
is asnp
is mentioned by
dbSNPrs794729108
ebirs794729108
HLIrs794729108
Exacrs794729108
Varsomers794729108
Maprs794729108
PheGenIrs794729108
hapmaprs794729108
1000 genomesrs794729108
hgdprs794729108
ensemblrs794729108
gopubmedrs794729108
geneviewrs794729108
scholarrs794729108
googlers794729108
pharmgkbrs794729108
gwascentralrs794729108
openSNPrs794729108
23andMers794729108
23andMe allrs794729108
SNP Nexus

SNPshotrs794729108
SNPdbers794729108
MSV3drs794729108
GWAS Ctlgrs794729108
Max Magnitude0
ClinVar
Risk rs794729108(G;G)
Alt rs794729108(G;G)
Reference rs794729108(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32977018A>C
CLNSRC
CLNACC RCV000183755.2,