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rs794729100

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729100(C;C)
Make rs794729100(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32792690
GenePKP2
is asnp
is mentioned by
dbSNPrs794729100
ebirs794729100
HLIrs794729100
Exacrs794729100
Varsomers794729100
Maprs794729100
PheGenIrs794729100
hapmaprs794729100
1000 genomesrs794729100
hgdprs794729100
ensemblrs794729100
gopubmedrs794729100
geneviewrs794729100
scholarrs794729100
googlers794729100
pharmgkbrs794729100
gwascentralrs794729100
openSNPrs794729100
23andMers794729100
23andMe allrs794729100
SNP Nexus

SNPshotrs794729100
SNPdbers794729100
MSV3drs794729100
GWAS Ctlgrs794729100
Max Magnitude0
ClinVar
Risk rs794729100(C;C)
Alt rs794729100(C;C)
Reference rs794729100(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32945624A>G
CLNSRC
CLNACC RCV000183718.1,