Source: ALL

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: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.830 1.000 6 2009 2017
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.710 1.000 2 2015 2019
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2016 2016
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0027697
Disease: Nephritis
Nephritis
0.010 1.000 1 2010 2010
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0003864
Disease: Arthritis
Arthritis
0.010 1.000 1 2019 2019
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.010 1.000 1 2012 2012
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0042384
Disease: Vasculitis
Vasculitis
0.010 1.000 1 2010 2010
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2012 2012