rs143044921, FREM2

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Bilateral hydronephrosis
CUI: C0521622
Disease: Bilateral hydronephrosis
3 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Congenital diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
31 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
36 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
80 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Diaphragmatic Eventration
CUI: C0011981
Disease: Diaphragmatic Eventration
6 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Hernia, Inguinal
CUI: C0019294
Disease: Hernia, Inguinal
21 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Umbilical hernia
CUI: C0019322
Disease: Umbilical hernia
17 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0