rs61729366, FRAS1

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Bilateral hydronephrosis
CUI: C0521622
Disease: Bilateral hydronephrosis
0.700 SusceptibilityMutation CLINVAR
Hernia, Inguinal
CUI: C0019294
Disease: Hernia, Inguinal
0.700 SusceptibilityMutation CLINVAR
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
0.700 SusceptibilityMutation CLINVAR
Congenital diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
0.700 SusceptibilityMutation CLINVAR
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
0.700 SusceptibilityMutation CLINVAR
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
0.700 SusceptibilityMutation CLINVAR