rs7528684, FCRL3

N. diseases: 10
Source: BEFREE ×
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
676 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.050 1.000 5 2006 2016
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
213 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.020 1.000 2 2013 2014
Endometriosis
CUI: C0014175
Disease: Endometriosis
207 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.020 1.000 2 2012 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
252 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.020 1.000 2 2010 2013
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
635 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.020 1.000 2 2013 2014
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
96 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Asthma
CUI: C0004096
Disease: Asthma
714 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
202 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
448 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015