rs3761959, FCRL3

N. diseases: 7
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.810 1.000 2 2011 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.710 1.000 2 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.710 1.000 2 2006 2015
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015