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rs769220833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs769220833(-;A)
Make rs769220833(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878346
GenePKP2
is asnp
is mentioned by
dbSNPrs769220833
dbSNP (old)rs769220833
ClinGenrs769220833
ebirs769220833
HLIrs769220833
Exacrs769220833
Varsomers769220833
Maprs769220833
PheGenIrs769220833
Biobankrs769220833
1000 genomesrs769220833
hgdprs769220833
ensemblrs769220833
gopubmedrs769220833
geneviewrs769220833
scholarrs769220833
googlers769220833
pharmgkbrs769220833
gwascentralrs769220833
openSNPrs769220833
23andMers769220833
23andMe allrs769220833
SNP Nexus

SNPshotrs769220833
SNPdbers769220833
MSV3drs769220833
GWAS Ctlgrs769220833
Max Magnitude0
ClinVar
Risk rs769220833(A;A)
Alt rs769220833(A;A)
Reference Rs769220833(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33031281dupA
CLNSRC
CLNACC RCV000183782.1,