rs3763747
|
0.925 |
0.120 |
10 |
59652577 |
3 prime UTR variant |
A/G
|
snv
|
|
0.21
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs3763747
|
0.925 |
0.120 |
10 |
59652577 |
3 prime UTR variant |
A/G
|
snv
|
|
0.21
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs12356193
|
0.925 |
0.120 |
10 |
59653595 |
intron variant |
A/G
|
snv
|
|
0.12
|
Uric acid measurement (procedure)
|
|
0.800 |
1.000 |
1 |
2009 |
2009 |
rs12356193
|
0.925 |
0.120 |
10 |
59653595 |
intron variant |
A/G
|
snv
|
|
0.12
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs12356193
|
0.925 |
0.120 |
10 |
59653595 |
intron variant |
A/G
|
snv
|
|
0.12
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs2242206
|
0.925 |
0.120 |
10 |
59654253 |
missense variant |
G/T
|
snv
|
0.34
|
0.25
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs2242206
|
0.925 |
0.120 |
10 |
59654253 |
missense variant |
G/T
|
snv
|
0.34
|
0.25
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1904071
|
0.925 |
0.120 |
10 |
59658933 |
intron variant |
T/C;G
|
snv
|
|
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1904071
|
0.925 |
0.120 |
10 |
59658933 |
intron variant |
T/C;G
|
snv
|
|
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs4948351
|
0.925 |
0.120 |
10 |
59665431 |
intron variant |
C/T
|
snv
|
|
0.19
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs4948351
|
0.925 |
0.120 |
10 |
59665431 |
intron variant |
C/T
|
snv
|
|
0.19
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs11006679
|
0.925 |
0.120 |
10 |
59668888 |
intron variant |
A/G
|
snv
|
|
0.66
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs11006679
|
0.925 |
0.120 |
10 |
59668888 |
intron variant |
A/G
|
snv
|
|
0.66
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs10826342
|
0.925 |
0.120 |
10 |
59673534 |
intron variant |
T/G
|
snv
|
|
0.66
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs10826342
|
0.925 |
0.120 |
10 |
59673534 |
intron variant |
T/G
|
snv
|
|
0.66
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171606
|
0.925 |
0.120 |
10 |
59674761 |
intron variant |
G/A;T
|
snv
|
|
|
Acylcarnitines measurement
|
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1171606
|
0.925 |
0.120 |
10 |
59674761 |
intron 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 |
2013 |
2013 |
rs1171606
|
0.925 |
0.120 |
10 |
59674761 |
intron 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 |
2013 |
2013 |
rs12772586
|
0.925 |
0.120 |
10 |
59680546 |
intron variant |
T/C
|
snv
|
|
0.12
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs12772586
|
0.925 |
0.120 |
10 |
59680546 |
intron variant |
T/C
|
snv
|
|
0.12
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171660
|
0.925 |
0.120 |
10 |
59684050 |
intron variant |
A/G
|
snv
|
0.44
|
0.41
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171660
|
0.925 |
0.120 |
10 |
59684050 |
intron variant |
A/G
|
snv
|
0.44
|
0.41
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171659
|
0.925 |
0.120 |
10 |
59684606 |
intron variant |
A/G
|
snv
|
|
0.31
|
CUI: |
C0018099 |
Disease: |
Gout
|
Gout
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171659
|
0.925 |
0.120 |
10 |
59684606 |
intron variant |
A/G
|
snv
|
|
0.31
|
Arthritis, Gouty
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1171659
|
0.925 |
0.120 |
10 |
59684606 |
intron variant |
A/G
|
snv
|
|
0.31
|
Uric acid measurement (procedure)
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |