rs1057524237, COL11A1

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cutis verticis gyrata
CUI: C0263417
Disease: Cutis verticis gyrata
0.700 CausalMutation CLINVAR
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.700 CausalMutation CLINVAR
Marshall syndrome
CUI: C0265235
Disease: Marshall syndrome
0.700 CausalMutation CLINVAR
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
0.700 CausalMutation CLINVAR
Orbital separation excessive
CUI: C0020534
Disease: Orbital separation excessive
0.700 CausalMutation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 CausalMutation CLINVAR
Thick upper lip vermilion
CUI: C1846423
Disease: Thick upper lip vermilion
0.700 CausalMutation CLINVAR