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 |
rs11231825
|
0.827 |
0.240 |
11 |
64592802 |
synonymous variant |
T/C
|
snv
|
0.57
|
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 |
rs3825016
|
0.882 |
0.160 |
11 |
64591814 |
synonymous variant |
C/T
|
snv
|
0.57
|
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 |
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 |
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
|
|
|
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
|
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
|
|
|
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 |
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 |