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: C0002171
Disease: Alopecia Areata
Alopecia Areata 		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: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		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: C0002170
Disease: Alopecia
Alopecia 		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: 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: 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: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult 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: 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: C0005411
Disease: Biliary Atresia
Biliary Atresia 		0.010 < 0.001 1 2017 2017
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		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: C4520983
Disease: Congenital atresia of extrahepatic bile duct
Congenital atresia of extrahepatic bile duct 		0.010 < 0.001 1 2017 2017
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: 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: 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: 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
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
0.611 0.720 22 23894205 intron variant G/C snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart 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: 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: 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: 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: 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: 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: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2016 2016