Source: GWASCAT

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: rs10821936
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.810 1.000 4 2009 2019
dbSNP: rs4948496
rs4948496
ARID5B
0.925 0.120 10 62045858 intron variant T/C snv 0.55
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 1.000 3 2013 2016
dbSNP: rs12764378
rs12764378
ARID5B
1.000 0.120 10 62040245 intron variant G/A snv 0.18
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2012 2015
dbSNP: rs7089424
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.800 1.000 2 2009 2018
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs10821944
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2012 2012
dbSNP: rs7090871
rs7090871
ARID5B
10 62070527 intron variant T/C snv 0.33
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.800 1.000 1 2013 2013
dbSNP: rs35809595
rs35809595
ARID5B
10 62072169 intron variant G/A snv 0.33
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.700 1.000 2 2018 2019
dbSNP: rs10821944
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10821944
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs10821950
rs10821950
ARID5B
10 62052208 intron variant T/C snv 0.45
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs10821953
rs10821953
ARID5B
10 62069120 intron variant T/A snv 0.33
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs12778514
rs12778514
ARID5B
10 62072520 intron variant G/A snv 0.33
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs2393730
rs2393730
ARID5B
10 62077247 intron variant G/A snv 0.33
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs4245595
rs4245595
ARID5B
1.000 0.120 10 61963136 intron variant C/T snv 0.69
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.700 1.000 1 2014 2014
dbSNP: rs4948492
rs4948492
ARID5B
10 61959980 intron variant C/T snv 0.69
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs5785510
rs5785510
ARID5B
10 62077531 intron variant AA/-;A;AAA delins
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2017 2017
dbSNP: rs7087507
rs7087507
ARID5B
0.925 0.120 10 61985930 intron variant A/G snv 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7089424
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma 		0.700 1.000 1 2018 2018
dbSNP: rs7090445
rs7090445
ARID5B
0.925 0.120 10 61961417 intron variant C/G;T snv 0.70
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma 		0.700 1.000 1 2013 2013
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs71508903
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019