CENPF, centromere protein F, 1063

N. diseases: 76; N. variants: 10
Disease: Jejunal Atresia with Microcephaly and Ocular Anomalies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200976140
rs200976140
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 CausalMutation CLINVAR
dbSNP: rs367624766
rs367624766
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 CausalMutation CLINVAR
dbSNP: rs376767238
rs376767238
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		C 0.700 CausalMutation CLINVAR
dbSNP: rs757531591
rs757531591
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs757575602
rs757575602
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 CausalMutation CLINVAR
dbSNP: rs776697039
rs776697039
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs779120472
rs779120472
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs786205697
rs786205697
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 CausalMutation CLINVAR
dbSNP: rs869312748
rs869312748
Entrez Id: 1063
Gene Symbol: CENPF
CENPF
CUI: C1855705
Disease:
Jejunal Atresia with Microcephaly and Ocular Anomalies 		T 0.700 CausalMutation CLINVAR