Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		0.020 1.000 2 2010 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0029453
Disease: Osteopenia
Osteopenia 		0.010 1.000 1 2010 2010
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		0.010 1.000 1 2011 2011
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2011 2011
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0003864
Disease: Arthritis
Arthritis 		0.030 1.000 3 2012 2020
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 1.000 2 2012 2020
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0038363
Disease: Aphthous Stomatitis
Aphthous Stomatitis 		0.010 1.000 1 2012 2012
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome 		0.010 1.000 1 2013 2013
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0018681
Disease: Headache
Headache 		0.010 1.000 1 2013 2013
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2014 2014
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0018021
Disease: Goiter
Goiter 		0.010 1.000 1 2014 2014
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.010 1.000 1 2014 2014
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 1.000 1 2014 2014
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0340164
Disease: Lofgrens syndrome
Lofgrens syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2015 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2015 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		0.010 1.000 1 2015 2015
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis 		0.010 < 0.001 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis 		0.010 1.000 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0025295
Disease: Meningitis, Pneumococcal
Meningitis, Pneumococcal 		0.010 1.000 1 2016 2016
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		0.010 1.000 1 2016 2016