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rs754912778

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754912778(A;A)
Make rs754912778(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32869034
GenePKP2
is asnp
is mentioned by
dbSNPrs754912778
ebirs754912778
HLIrs754912778
Exacrs754912778
Varsomers754912778
Maprs754912778
PheGenIrs754912778
hapmaprs754912778
1000 genomesrs754912778
hgdprs754912778
ensemblrs754912778
gopubmedrs754912778
geneviewrs754912778
scholarrs754912778
googlers754912778
pharmgkbrs754912778
gwascentralrs754912778
openSNPrs754912778
23andMers754912778
23andMe allrs754912778
SNP Nexus

SNPshotrs754912778
SNPdbers754912778
MSV3drs754912778
GWAS Ctlgrs754912778
Max Magnitude0
ClinVar
Risk rs754912778(A;A)
Alt rs754912778(A;A)
Reference rs754912778(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33021968G>A
CLNSRC
CLNACC RCV000183731.2,