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rs794729099

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729099(C;T)
Make rs794729099(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32792699
GenePKP2
is asnp
is mentioned by
dbSNPrs794729099
ebirs794729099
HLIrs794729099
Exacrs794729099
Varsomers794729099
Maprs794729099
PheGenIrs794729099
hapmaprs794729099
1000 genomesrs794729099
hgdprs794729099
ensemblrs794729099
gopubmedrs794729099
geneviewrs794729099
scholarrs794729099
googlers794729099
pharmgkbrs794729099
gwascentralrs794729099
openSNPrs794729099
23andMers794729099
23andMe allrs794729099
SNP Nexus

SNPshotrs794729099
SNPdbers794729099
MSV3drs794729099
GWAS Ctlgrs794729099
Max Magnitude0
ClinVar
Risk rs794729099(T;T)
Alt rs794729099(T;T)
Reference rs794729099(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32945633G>A
CLNSRC
CLNACC RCV000183717.2,