rs1106766
|
0.882 |
0.120 |
12 |
57415673 |
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 |
2 |
2010 |
2013 |
rs11172147
|
0.925 |
0.120 |
12 |
57302894 |
intron variant |
G/A
|
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 |
2 |
2010 |
2013 |
rs11609805
|
0.925 |
0.120 |
12 |
57341262 |
5 prime UTR variant |
G/A;C;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 |
rs11613352
|
0.827 |
0.160 |
12 |
57398797 |
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 |
2 |
2010 |
2013 |
rs11614506
|
0.925 |
0.120 |
12 |
57421892 |
intron variant |
T/C
|
snv
|
|
0.16
|
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 |
rs4760254
|
0.925 |
0.120 |
12 |
57372609 |
intron variant |
G/A;C;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 |
rs4760278
|
0.925 |
0.120 |
12 |
57377370 |
intron variant |
C/A
|
snv
|
|
0.16
|
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 |
rs4760355
|
0.925 |
0.120 |
12 |
57331414 |
intron variant |
G/A
|
snv
|
|
0.20
|
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 |
rs7964492
|
0.925 |
0.120 |
12 |
57429802 |
intron variant |
A/C
|
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 |
2 |
2010 |
2013 |