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rs794729132

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729132(C;T)
Make rs794729132(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878483
GenePKP2
is asnp
is mentioned by
dbSNPrs794729132
ebirs794729132
HLIrs794729132
Exacrs794729132
Varsomers794729132
Maprs794729132
PheGenIrs794729132
hapmaprs794729132
1000 genomesrs794729132
hgdprs794729132
ensemblrs794729132
gopubmedrs794729132
geneviewrs794729132
scholarrs794729132
googlers794729132
pharmgkbrs794729132
gwascentralrs794729132
openSNPrs794729132
23andMers794729132
23andMe allrs794729132
SNP Nexus

SNPshotrs794729132
SNPdbers794729132
MSV3drs794729132
GWAS Ctlgrs794729132
Max Magnitude0
ClinVar
Risk rs794729132(T;T)
Alt rs794729132(T;T)
Reference rs794729132(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33031417G>A
CLNSRC
CLNACC RCV000183801.1,