rs12583006, TNFSF13B

N. diseases: 8
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.
Hepatitis
CUI: C0019158
Disease: Hepatitis
42 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1 2017 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2017 2017
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.807 0.320 13 108285104 intron variant T/A snv 0.21 0.010 1.000 1 2014 2014