rs505802
0.882
0.160
11
64589600
upstream gene variant
T/C
snv
0.45
Uric acid measurement (procedure)
0.800
1.000
3
2009
2019
rs505802
0.882
0.160
11
64589600
upstream gene variant
T/C
snv
0.45
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.710
1.000
3
2010
2015
rs10897518
0.925
0.120
11
64593233
intron variant
C/T
snv
0.51
Uric acid measurement (procedure)
0.800
1.000
2
2009
2015
rs10897518
0.925
0.120
11
64593233
intron variant
C/T
snv
0.51
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs10897518
0.925
0.120
11
64593233
intron variant
C/T
snv
0.51
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs1451506414
0.882
0.200
11
64598561
synonymous variant
G/A
snv
Renal hypouricemia
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
0.020
1.000
2
2008
2011
rs3825018
0.925
0.120
11
64591337
5 prime UTR variant
G/A
snv
0.51
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs3825018
0.925
0.120
11
64591337
5 prime UTR variant
G/A
snv
0.51
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs475688
0.882
0.160
11
64596819
intron variant
C/T
snv
0.25
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs475688
0.882
0.160
11
64596819
intron variant
C/T
snv
0.25
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs505802
0.882
0.160
11
64589600
upstream gene variant
T/C
snv
0.45
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs524023
0.925
0.120
11
64590793
5 prime UTR variant
C/G;T
snv
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs524023
0.925
0.120
11
64590793
5 prime UTR variant
C/G;T
snv
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs893006
0.882
0.160
11
64598324
intron variant
C/A
snv
0.61
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs893006
0.882
0.160
11
64598324
intron variant
C/A
snv
0.61
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs9734313
0.925
0.120
11
64590839
5 prime UTR variant
C/G;T
snv
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs9734313
0.925
0.120
11
64590839
5 prime UTR variant
C/G;T
snv
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
2
2010
2013
rs11602903
0.882
0.120
11
64590769
5 prime UTR variant
A/T
snv
0.51
Essential Hypertension
Cardiovascular Diseases
0.010
1.000
1
2012
2012
rs11602903
0.882
0.120
11
64590769
5 prime UTR variant
A/T
snv
0.51
Hyperuricemia
Pathological Conditions, Signs and Symptoms
0.010
1.000
1
2015
2015
rs11602903
0.882
0.120
11
64590769
5 prime UTR variant
A/T
snv
0.51
Metabolic Syndrome X
Nutritional and Metabolic Diseases
0.010
1.000
1
2012
2012
rs1230053514
1.000
0.040
11
64598551
missense variant
C/T
snv
Hyperuricemia
Pathological Conditions, Signs and Symptoms
0.010
1.000
1
2011
2011
rs12800450
0.925
0.120
11
64591749
missense variant
G/A;T
snv
×
CUI:
C0018099
Disease:
Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
1
2011
2011
rs12800450
0.925
0.120
11
64591749
missense variant
G/A;T
snv
Uric acid measurement (procedure)
0.700
1.000
1
2011
2011
rs12800450
0.925
0.120
11
64591749
missense variant
G/A;T
snv
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
0.700
1.000
1
2011
2011
rs1451506414
0.882
0.200
11
64598561
synonymous variant
G/A
snv
Hypouricemia
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
0.010
1.000
1
2008
2008