rs1057518891, CHD7

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
0.700 CausalMutation CLINVAR
Long narrow head
CUI: C0221358
Disease: Long narrow head
0.700 CausalMutation CLINVAR
Progressive hearing impairment
CUI: C1842138
Disease: Progressive hearing impairment
0.700 CausalMutation CLINVAR
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.700 CausalMutation CLINVAR
Myopia
CUI: C0027092
Disease: Myopia
0.700 CausalMutation CLINVAR
Poor coordination
CUI: C0563243
Disease: Poor coordination
0.700 CausalMutation CLINVAR