INCENP, inner centromere protein, 3619

N. diseases: 24; N. variants: 4
Disease: Nephronophthisis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61893682
rs61893682
Entrez Id: 3619
Gene Symbol: INCENP
INCENP
CUI: C0687120
Disease:
Nephronophthisis 		C 0.700 GeneticVariation CLINVAR Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. 26489029 2016