rs10774624, LINC02356

N. diseases: 6
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.810 1.000 3 2014 2019
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
Tonometry
CUI: C0040420
Disease: Tonometry
573 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2018 2018
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.010 1.000 1 2017 2017