rs61361928, UGT2B7

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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 1.000 0.040 4 69096657 missense variant T/C snv 2.6E-03 2.8E-03 0.700 1.000 1 2015 2015