rs67865220
|
0.851 |
0.120 |
7 |
94409795 |
missense variant |
G/A;C;T
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.800 |
|
0 |
|
|
rs121912911
|
0.925 |
0.200 |
7 |
94426442 |
missense variant |
G/C
|
snv
|
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.710 |
1.000 |
1 |
1996 |
1996 |
rs66773001
|
0.882 |
0.120 |
7 |
94410251 |
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 |
1.000 |
15 |
1991 |
2006 |
rs66883877
|
0.882 |
0.160 |
7 |
94419499 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06
|
1.4E-05
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
15 |
1991 |
2006 |
rs72658186
|
1.000 |
0.120 |
7 |
94421045 |
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 |
1.000 |
15 |
1991 |
2006 |
rs72658191
|
1.000 |
0.120 |
7 |
94423011 |
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 |
1.000 |
15 |
1991 |
2006 |
rs1114167412
|
1.000 |
0.120 |
7 |
94410492 |
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 |
1.000 |
1 |
2015 |
2015 |
rs1114167414
|
0.925 |
0.120 |
7 |
94426433 |
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 |
1.000 |
1 |
2015 |
2015 |
rs1114167415
|
0.925 |
0.120 |
7 |
94426514 |
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 |
1.000 |
1 |
2015 |
2015 |
rs67609234
|
1.000 |
0.120 |
7 |
94425832 |
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 |
1.000 |
1 |
2015 |
2015 |
rs67729041
|
1.000 |
0.120 |
7 |
94409778 |
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 |
1.000 |
1 |
2015 |
2015 |
rs72658150
|
1.000 |
0.120 |
7 |
94417797 |
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 |
1.000 |
1 |
2015 |
2015 |
rs121912905
|
0.925 |
0.120 |
7 |
94408806 |
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 |
|
|
rs121912907
|
0.925 |
0.120 |
7 |
94415263 |
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 |
|
|
rs1554396283
|
1.000 |
0.120 |
7 |
94410926 |
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 |
|
|
rs1800250
|
1.000 |
0.120 |
7 |
94427801 |
missense variant |
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 |
|
|
rs267606742
|
1.000 |
0.120 |
7 |
94427628 |
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 |
|
|
rs66612022
|
0.763 |
0.240 |
7 |
94409768 |
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 |
|
|
rs66619856
|
0.882 |
0.120 |
7 |
94410278 |
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 |
|
|
rs67543427
|
0.776 |
0.240 |
7 |
94410457 |
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 |
|
|
rs72656402
|
1.000 |
0.120 |
7 |
94410429 |
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 |
|
|
rs72658118
|
0.882 |
0.120 |
7 |
94412095 |
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 |
|
|
rs72658126
|
1.000 |
0.120 |
7 |
94413128 |
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 |
|
|
rs72658176
|
0.882 |
0.120 |
7 |
94420604 |
missense variant |
G/A
|
snv
|
4.1E-06
|
|
Osteogenesis imperfecta type III (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs72658200
|
1.000 |
0.120 |
7 |
94424345 |
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 |
|
|