rs1553827236, CC2D2A

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Encephalocele
CUI: C4551722
Disease: Encephalocele
0.700 CausalMutation CLINVAR
POLYDACTYLY, POSTAXIAL
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
0.700 CausalMutation CLINVAR
Congenital clubfoot
CUI: C0009081
Disease: Congenital clubfoot
0.700 CausalMutation CLINVAR
Narrow thorax
CUI: C0426790
Disease: Narrow thorax
0.700 CausalMutation CLINVAR
Polycystic Kidney Diseases
CUI: C0022680
Disease: Polycystic Kidney Diseases
0.700 CausalMutation CLINVAR
Microcephaly (physical finding)
CUI: C4551563
Disease: Microcephaly (physical finding)
0.700 CausalMutation CLINVAR
Oligohydramnios
CUI: C0079924
Disease: Oligohydramnios
0.700 CausalMutation CLINVAR