CENPJ, centromere protein J, 55835

N. diseases: 150; N. variants: 24
Disease: Microcephaly, Primary Autosomal Recessive, 6 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202058504
rs202058504
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
CUI: C1842109
Disease:
Microcephaly, Primary Autosomal Recessive, 6 		C 0.700 CausalMutation CLINVAR
dbSNP: rs202058504
rs202058504
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
CUI: C1842109
Disease:
Microcephaly, Primary Autosomal Recessive, 6 		C 0.700 GeneticVariation CLINVAR