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: 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: 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: 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: 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: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.020 1.000 2 2017 2019
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.020 1.000 2 2018 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.010 1.000 1 2018 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.010 1.000 1 2018 2018
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0265962
Disease: Ichthyosis linearis circumflexa
Ichthyosis linearis circumflexa 		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: 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: 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: C0022650
Disease: Kidney Calculi
Kidney Calculi 		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: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic 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: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2017 2017
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: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis 		0.010 1.000 1 2017 2017
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: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2017 2017
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: 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: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2019 2019
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