rs533297350, COL4A4

N. diseases: 5
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.
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0
Hematuria
CUI: C0018965
Disease: Hematuria
31 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0
Myopia
CUI: C0027092
Disease: Myopia
167 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0
Proteinuria
CUI: C0033687
Disease: Proteinuria
20 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0