rs4810485, CD40

N. diseases: 16
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 0.732 0.480 20 46119308 intron variant T/A;G snv 0.840 1.000 7 2008 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.732 0.480 20 46119308 intron variant T/A;G snv 0.810 1.000 3 2011 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.732 0.480 20 46119308 intron variant T/A;G snv 0.770 1.000 8 2011 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.732 0.480 20 46119308 intron variant T/A;G snv 0.710 1.000 2 2011 2016
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.732 0.480 20 46119308 intron variant T/A;G snv 0.700 1.000 1 2011 2011
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.732 0.480 20 46119308 intron variant T/A;G snv 0.020 1.000 2 2012 2015
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2011 2011
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2019 2019
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2011 2011
Recurrent aphthous ulcer
CUI: C2937365
Disease: Recurrent aphthous ulcer
22 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2015 2015