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rs794729106

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729106(C;C)
Make rs794729106(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32850766
GenePKP2
is asnp
is mentioned by
dbSNPrs794729106
ebirs794729106
HLIrs794729106
Exacrs794729106
Varsomers794729106
Maprs794729106
PheGenIrs794729106
hapmaprs794729106
1000 genomesrs794729106
hgdprs794729106
ensemblrs794729106
gopubmedrs794729106
geneviewrs794729106
scholarrs794729106
googlers794729106
pharmgkbrs794729106
gwascentralrs794729106
openSNPrs794729106
23andMers794729106
23andMe allrs794729106
SNP Nexus

SNPshotrs794729106
SNPdbers794729106
MSV3drs794729106
GWAS Ctlgrs794729106
Max Magnitude0
ClinVar
Risk rs794729106(C;C)
Alt rs794729106(C;C)
Reference rs794729106(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33003700C>G
CLNSRC
CLNACC RCV000183742.1,