rs17368443, SBF2

N. diseases: 1
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 11 10275289 intron variant G/C snv 5.3E-02 0.700 1.000 1 2018 2018