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rs794729103

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729103(C;T)
Make rs794729103(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878363
GenePKP2
is asnp
is mentioned by
dbSNPrs794729103
ebirs794729103
HLIrs794729103
Exacrs794729103
Varsomers794729103
Maprs794729103
PheGenIrs794729103
hapmaprs794729103
1000 genomesrs794729103
hgdprs794729103
ensemblrs794729103
gopubmedrs794729103
geneviewrs794729103
scholarrs794729103
googlers794729103
pharmgkbrs794729103
gwascentralrs794729103
openSNPrs794729103
23andMers794729103
23andMe allrs794729103
SNP Nexus

SNPshotrs794729103
SNPdbers794729103
MSV3drs794729103
GWAS Ctlgrs794729103
Max Magnitude0
ClinVar
Risk rs794729103(T;T)
Alt rs794729103(T;T)
Reference rs794729103(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33031297G>A
CLNSRC
CLNACC RCV000183727.1,