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: rs1007888
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.020 1.000 2 2011 2015
dbSNP: rs5844572
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins
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: 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: 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: 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: 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: 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: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		0.020 1.000 2 2010 2018
dbSNP: rs1007888
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1007888
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2011 2011
dbSNP: rs1007888
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2009 2009
dbSNP: rs10433310
rs10433310
MIF-AS1
1.000 0.080 22 23896636 intron variant G/A snv 0.32
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		0.010 1.000 1 2012 2012
dbSNP: rs11548059
rs11548059
MIF ; MIF-AS1
0.925 0.080 22 23894794 missense variant C/G;T snv 6.1E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 < 0.001 1 2017 2017
dbSNP: rs11548059
rs11548059
MIF ; MIF-AS1
0.925 0.080 22 23894794 missense variant C/G;T snv 6.1E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 < 0.001 1 2017 2017
dbSNP: rs1803976
rs1803976
MIF ; MIF-AS1
0.925 0.080 22 23895075 missense variant A/G snv 3.0E-05 4.2E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 < 0.001 1 2017 2017
dbSNP: rs1803976
rs1803976
MIF ; MIF-AS1
0.925 0.080 22 23895075 missense variant A/G snv 3.0E-05 4.2E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 < 0.001 1 2017 2017
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome 		0.010 1.000 1 2013 2013
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C0018681
Disease: Headache
Headache 		0.010 1.000 1 2013 2013
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.010 1.000 1 2013 2013
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs2096525
rs2096525
MIF ; MIF-AS1
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 1.000 1 2013 2013
dbSNP: rs34383331
rs34383331
MIF-AS1
0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18
CUI: C0024530
Disease: Malaria
Malaria 		0.010 1.000 1 2013 2013
dbSNP: rs34383331
rs34383331
MIF-AS1
0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18
CUI: C0024535
Disease: Malaria, Falciparum
Malaria, Falciparum 		0.010 1.000 1 2013 2013