Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.720 0.667 2 2011 2017
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.100 0.818 11 2007 2018
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.050 1.000 5 2008 2019
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.040 1.000 4 2009 2015
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 0.667 3 2015 2017
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.030 1.000 3 2012 2015
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.020 1.000 2 2008 2012
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.020 1.000 2 2009 2013
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C1853829
Disease: Arthropathy, Erosive
Arthropathy, Erosive 		0.010 1.000 1 2015 2015
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.010 1.000 1 2016 2016
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C1519176
Disease: Salivary Gland Pleomorphic Adenoma
Salivary Gland Pleomorphic Adenoma 		0.010 1.000 1 2008 2008
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2011 2011
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2011 2011
dbSNP: rs6887695
rs6887695 		0.732 0.440 5 159395637 intron variant G/C snv 0.35
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2014 2014