rs9514828, TNFSF13B

N. diseases: 12
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.
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.020 1.000 2 2015 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.020 0.500 2 2017 2019
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.020 1.000 2 2012 2012
B-CELL MALIGNANCY, LOW-GRADE
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
19 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2015 2015
BAFF polymorphism
CUI: C3888909
Disease: BAFF polymorphism
2 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2017 2017
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2019 2019
Hepatitis
CUI: C0019158
Disease: Hepatitis
42 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1 2017 2017
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2017 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2019 2019
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014