rs8182352, None

N. diseases: 5
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.
Alveolitis, Fibrosing
CUI: C4721507
Disease: Alveolitis, Fibrosing
4 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 0.010 1.000 1 2011 2011
Generalized vitiligo
CUI: C1304470
Disease: Generalized vitiligo
16 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 0.010 1.000 1 2007 2007
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
8 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 0.010 1.000 1 2011 2011
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 0.010 1.000 1 2011 2011
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 0.010 1.000 1 2011 2011