Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729135

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729135(G;T)
Make rs794729135(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32822583
GenePKP2
is asnp
is mentioned by
dbSNPrs794729135
ebirs794729135
HLIrs794729135
Exacrs794729135
Varsomers794729135
Maprs794729135
PheGenIrs794729135
hapmaprs794729135
1000 genomesrs794729135
hgdprs794729135
ensemblrs794729135
gopubmedrs794729135
geneviewrs794729135
scholarrs794729135
googlers794729135
pharmgkbrs794729135
gwascentralrs794729135
openSNPrs794729135
23andMers794729135
23andMe allrs794729135
SNP Nexus

SNPshotrs794729135
SNPdbers794729135
MSV3drs794729135
GWAS Ctlgrs794729135
Max Magnitude0
ClinVar
Risk rs794729135(T;T)
Alt rs794729135(T;T)
Reference rs794729135(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32975517C>A
CLNSRC
CLNACC RCV000183809.1,