CEP97, centrosomal protein 97, 79598

N. diseases: 4; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060499739
rs1060499739
Entrez Id: 79598
Gene Symbol: CEP97
CEP97
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1060499739
rs1060499739
Entrez Id: 79598
Gene Symbol: CEP97
CEP97
CUI: C0557874
Disease:
Global developmental delay 		G 0.700 GeneticVariation CLINVAR