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: rs2231142
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0018099
Disease: Gout
Gout 		0.820 1.000 6 2008 2019
dbSNP: rs2231142
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.810 1.000 6 2008 2019
dbSNP: rs2231142
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 14 2008 2019
dbSNP: rs4148155
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 3 2009 2019
dbSNP: rs1481012
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 2 2009 2019
dbSNP: rs2054576
rs2054576
ABCG2
0.882 0.160 4 88107623 intron variant A/G snv 7.8E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 2 2009 2019
dbSNP: rs3114018
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 2 2009 2018
dbSNP: rs4148155
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.800 1.000 2 2010 2019
dbSNP: rs4148155
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02
CUI: C0018099
Disease: Gout
Gout 		0.800 1.000 2 2010 2019
dbSNP: rs10011796
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 1 2009 2015
dbSNP: rs10011796
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.800 1.000 1 2010 2015
dbSNP: rs10011796
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv
CUI: C0018099
Disease: Gout
Gout 		0.800 1.000 1 2010 2015
dbSNP: rs1481012
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C0018099
Disease: Gout
Gout 		0.800 1.000 1 2010 2013
dbSNP: rs1481012
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.800 1.000 1 2010 2013
dbSNP: rs2231142
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.800 1.000 1 2010 2019
dbSNP: rs3114018
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48
CUI: C0011334
Disease: Dental caries
Dental caries 		0.800 1.000 1 2013 2013
dbSNP: rs3114020
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40
CUI: C0018099
Disease: Gout
Gout 		0.800 1.000 1 2010 2017
dbSNP: rs3114020
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.800 1.000 1 2010 2017
dbSNP: rs2199936
rs2199936
ABCG2
0.882 0.160 4 88124179 intron variant A/G;T snv 0.88
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 4 2010 2019
dbSNP: rs1481012
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1481012
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C3549252
Disease: response to statin
response to statin 		0.700 1.000 1 2012 2012
dbSNP: rs1481014
rs1481014
ABCG2
0.882 0.160 4 88175999 intron variant C/A;T snv 0.24
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1481017
rs1481017
ABCG2
0.882 0.160 4 88176325 intron variant C/T snv 0.59
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1871744
rs1871744
ABCG2
0.925 0.120 4 88118477 intron variant T/C snv 0.15
CUI: C0018099
Disease: Gout
Gout 		0.700 1.000 1 2017 2017
dbSNP: rs1871744
rs1871744
ABCG2
0.925 0.120 4 88118477 intron variant T/C snv 0.15
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 1.000 1 2017 2017