rs499952, MRE11

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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.925 0.040 11 94449826 intron variant G/T snv 0.41 0.010 1.000 1 2019 2019
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.925 0.040 11 94449826 intron variant G/T snv 0.41 0.010 1.000 1 2019 2019