rs6651252, LINC00824

N. diseases: 8
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.810 1.000 6 2010 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 2 2015 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016