rs4263839, TNFSF15

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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.830 0.667 4 2008 2015
Asthma
CUI: C0004096
Disease: Asthma
729 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.700 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
745 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.700 1 2012 2012
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
36 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.020 0.500 2 2012 2016
Constipation
CUI: C0009806
Disease: Constipation
7 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.010 1.000 1 2012 2012
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
696 0.821 0.143 9 114804160 intron variant A/G snp 0.73 0.010 1.000 1 2015 2015