rs72659304
|
0.925 |
0.120 |
7 |
94425118 |
missense variant |
G/A
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659312
|
1.000 |
0.120 |
7 |
94425759 |
missense variant |
G/A
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659316
|
1.000 |
0.120 |
7 |
94426026 |
missense variant |
G/T
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659319
|
0.763 |
0.240 |
7 |
94426459 |
missense variant |
G/A;C
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659335
|
0.882 |
0.120 |
7 |
94427288 |
missense variant |
G/A;T
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659337
|
1.000 |
0.120 |
7 |
94427646 |
missense variant |
G/C
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659338
|
1.000 |
0.120 |
7 |
94427654 |
missense variant |
G/A
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72659345
|
1.000 |
0.120 |
7 |
94430291 |
frameshift variant |
ATAA/-
|
delins
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs768171831
|
0.882 |
0.120 |
7 |
94426011 |
missense variant |
C/T
|
snv
|
1.2E-04;
4.0E-06
|
5.6E-05
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72658125
|
1.000 |
0.120 |
7 |
94413110 |
missense variant |
G/A
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.010 |
1.000 |
1 |
2003 |
2003 |