rs61753185
|
0.882 |
0.160 |
11 |
89178183 |
missense variant |
G/A
|
snv
|
8.4E-05
|
5.6E-05
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
25 |
1990 |
2015 |
rs28940876
|
0.827 |
0.160 |
11 |
89178195 |
missense variant |
C/T
|
snv
|
8.4E-05
|
1.7E-04
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
21 |
1990 |
2014 |
rs61753180
|
0.882 |
0.160 |
11 |
89178093 |
missense variant |
G/A
|
snv
|
1.6E-04
|
2.8E-04
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
21 |
1990 |
2014 |
rs61754363
|
1.000 |
0.160 |
11 |
89178599 |
missense variant |
T/A;C
|
snv
|
1.6E-05;
8.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
1 |
1993 |
1993 |
rs121908011
|
0.827 |
0.160 |
11 |
89227933 |
missense variant |
G/A
|
snv
|
9.2E-05
|
3.5E-05
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
22 |
1990 |
2014 |
rs104894313
|
0.807 |
0.160 |
11 |
89284805 |
missense variant |
C/T
|
snv
|
3.8E-03;
4.0E-06
|
3.7E-03
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs104894314
|
0.790 |
0.160 |
11 |
89191205 |
missense variant |
G/A;T
|
snv
|
8.0E-06;
9.2E-05
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs104894315
|
1.000 |
0.160 |
11 |
89227932 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
6.8E-05
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs104894316
|
0.925 |
0.160 |
11 |
89284797 |
missense variant |
G/A;T
|
snv
|
4.0E-06;
3.6E-05
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs104894317
|
0.925 |
0.160 |
11 |
89284924 |
missense variant |
G/A
|
snv
|
4.0E-05
|
1.1E-04
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs104894318
|
1.000 |
0.160 |
11 |
89284930 |
missense variant |
G/A;C
|
snv
|
1.6E-05;
4.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs137854890
|
1.000 |
0.160 |
11 |
89178225 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs151206295
|
1.000 |
0.160 |
11 |
89227850 |
missense variant |
C/G;T
|
snv
|
1.6E-05;
1.4E-04
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs28940877
|
0.807 |
0.200 |
11 |
89178218 |
missense variant |
T/C
|
snv
|
4.0E-06
|
2.1E-05
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs28940878
|
1.000 |
0.160 |
11 |
89178078 |
missense variant |
A/G
|
snv
|
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs28940879
|
0.851 |
0.160 |
11 |
89178117 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs28940880
|
1.000 |
0.160 |
11 |
89178569 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs61753178
|
1.000 |
0.160 |
11 |
89178014 |
missense variant |
C/T
|
snv
|
3.6E-05
|
1.4E-05
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs61753184
|
1.000 |
0.160 |
11 |
89178182 |
missense variant |
C/T
|
snv
|
2.4E-05;
3.2E-05
|
6.3E-05
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs61754392
|
0.925 |
0.160 |
11 |
89284843 |
missense variant |
G/A
|
snv
|
6.4E-05
|
7.0E-06
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1990 |
2014 |
rs61754365
|
0.925 |
0.160 |
11 |
89178603 |
missense variant |
G/A;C;T
|
snv
|
2.6E-04;
1.2E-05
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
|
0 |
|
|
rs61754367
|
1.000 |
0.160 |
11 |
89178660 |
stop gained |
G/A;C
|
snv
|
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.800 |
|
0 |
|
|
rs281865325
|
0.925 |
0.160 |
11 |
89284880 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.710 |
1.000 |
21 |
1990 |
2014 |
rs61754388
|
0.827 |
0.160 |
11 |
89227904 |
missense variant |
C/A
|
snv
|
3.4E-04
|
5.0E-04
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.710 |
1.000 |
9 |
1990 |
2013 |
rs61754385
|
1.000 |
0.160 |
11 |
89227895 |
missense variant |
T/C
|
snv
|
|
|
Oculocutaneous albinism type 1A
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
0.710 |
1.000 |
1 |
2013 |
2013 |