rs2236295, ADO

N. diseases: 2
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.
Albuminuria
CUI: C0001925
Disease: Albuminuria
59 10 62805132 missense variant G/C;T snv 0.32 0.700 1.000 1 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 10 62805132 missense variant G/C;T snv 0.32 0.700 1.000 1 2019 2019