rs77543610
|
0.667 |
0.560 |
10 |
121520160 |
missense variant |
G/C
|
snv
|
|
|
Apert syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.900 |
1.000 |
8 |
1995 |
2018 |
rs121918499
|
0.925 |
0.160 |
10 |
121520048 |
missense variant |
C/A;G
|
snv
|
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.840 |
1.000 |
13 |
1995 |
2019 |
rs121918501
|
0.807 |
0.080 |
10 |
121520050 |
missense variant |
A/C;G
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.830 |
1.000 |
16 |
1994 |
2014 |
rs121918487
|
0.716 |
0.440 |
10 |
121517378 |
missense variant |
C/A;G;T
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.820 |
1.000 |
17 |
1994 |
2007 |
rs121918488
|
0.790 |
0.120 |
10 |
121517379 |
missense variant |
A/C;G;T
|
snv
|
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.820 |
1.000 |
17 |
1994 |
2015 |
rs121918496
|
0.851 |
0.120 |
10 |
121517377 |
missense variant |
G/C
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.820 |
1.000 |
16 |
1994 |
2007 |
rs121918502
|
0.790 |
0.160 |
10 |
121517351 |
missense variant |
G/C
|
snv
|
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.820 |
1.000 |
13 |
1995 |
2014 |
rs776587763
|
0.790 |
0.120 |
10 |
121520085 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
4.0E-06
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.820 |
1.000 |
13 |
1995 |
2014 |
rs121918488
|
0.790 |
0.120 |
10 |
121517379 |
missense variant |
A/C;G;T
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
16 |
1994 |
2012 |
rs121918490
|
0.851 |
0.080 |
10 |
121517342 |
missense variant |
G/C
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
16 |
1994 |
2007 |
rs121918492
|
0.882 |
0.080 |
10 |
121517372 |
missense variant |
G/C
|
snv
|
|
7.0E-06
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
16 |
1994 |
2007 |
rs121918497
|
0.776 |
0.160 |
10 |
121520052 |
missense variant |
T/G
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
16 |
1994 |
2007 |
rs121918505
|
0.851 |
0.080 |
10 |
121520119 |
missense variant |
A/G
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
16 |
1994 |
2019 |
rs121918487
|
0.716 |
0.440 |
10 |
121517378 |
missense variant |
C/A;G;T
|
snv
|
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
13 |
1995 |
2015 |
rs121918510
|
1.000 |
0.080 |
10 |
121517441 |
missense variant |
T/G
|
snv
|
|
|
Pfeiffer Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
13 |
1995 |
2007 |
rs121918498
|
1.000 |
0.080 |
10 |
121520162 |
missense variant |
CG/AA
|
mnv
|
|
|
Apert syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
8 |
1995 |
2004 |
rs121918492
|
0.882 |
0.080 |
10 |
121517372 |
missense variant |
G/C
|
snv
|
|
7.0E-06
|
JACKSON-WEISS SYNDROME
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.810 |
1.000 |
5 |
1994 |
1998 |
rs121913477
|
1.000 |
0.120 |
10 |
121515289 |
missense variant |
G/C;T
|
snv
|
|
|
Cutis Gyrata Syndrome of Beare And Stevenson
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.810 |
1.000 |
2 |
1996 |
2008 |
rs121913478
|
0.708 |
0.640 |
10 |
121515280 |
missense variant |
T/C
|
snv
|
|
|
Cutis Gyrata Syndrome of Beare And Stevenson
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.810 |
1.000 |
2 |
1996 |
2007 |
rs121918493
|
1.000 |
0.080 |
10 |
121517420 |
missense variant |
T/C
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
18 |
1994 |
2016 |
rs121918489
|
1.000 |
0.080 |
10 |
121517385 |
missense variant |
A/G
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
16 |
1994 |
2007 |
rs121918494
|
0.790 |
0.160 |
10 |
121517363 |
missense variant |
G/C
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
16 |
1994 |
2007 |
rs121918500
|
1.000 |
0.080 |
10 |
121520044 |
missense variant |
T/C
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
16 |
1994 |
2007 |
rs1554927408
|
0.742 |
0.480 |
10 |
121515254 |
missense variant |
C/T
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
16 |
1994 |
2007 |
rs387906676
|
1.000 |
0.080 |
10 |
121517394 |
missense variant |
C/G;T
|
snv
|
|
|
Craniofacial dysostosis type 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
0.800 |
1.000 |
16 |
1994 |
2007 |