rs10036748, TNIP1

N. diseases: 11
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.360 5 151078585 intron variant C/A;T snv 0.830 1.000 6 2009 2017
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.360 5 151078585 intron variant C/A;T snv 0.710 1.000 2 2015 2019
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2019 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2017 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2019 2019
Nephritis
CUI: C0027697
Disease: Nephritis
40 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2010 2010
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2012 2012
Vasculitis
CUI: C0042384
Disease: Vasculitis
24 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2010 2010