rs10499194, None

N. diseases: 10
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 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.880 1.000 8 2007 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.700 1.000 1 2011 2011
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
4 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2017 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2019 2019
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1 2010 2010
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2013 2013
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2017 2017
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2009 2009
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2010 2010
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1 2010 2010