rs911263, RAD51B

N. diseases: 4
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.800 1.000 3 2011 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.720 1.000 3 2013 2017
Biliary cirrhosis
CUI: C0023892
Disease: Biliary cirrhosis
36 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.700 1.000 1 2011 2011
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.700 1.000 1 2017 2017