rs35953626
|
1.000 |
0.120 |
4 |
5753797 |
missense variant |
G/A
|
snv
|
1.8E-02
|
7.1E-02
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
3 |
2000 |
2010 |
rs149898884
|
1.000 |
0.120 |
4 |
5756299 |
missense variant |
G/A
|
snv
|
3.9E-04
|
1.6E-03
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs121908426
|
0.925 |
0.160 |
4 |
5745321 |
missense variant |
T/C
|
snv
|
4.8E-05
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
3 |
2000 |
2013 |
rs121908425
|
0.763 |
0.160 |
4 |
5748226 |
stop gained |
C/A;T
|
snv
|
3.2E-05;
1.2E-05
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
3 |
2000 |
2018 |
rs779915989
|
1.000 |
0.120 |
4 |
5748268 |
stop gained |
G/A;T
|
snv
|
2.8E-05;
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs755381180
|
0.882 |
0.160 |
4 |
5745303 |
inframe deletion |
AAG/-
|
delins
|
1.6E-05
|
2.8E-05
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs527255616
|
0.925 |
0.160 |
4 |
5745274 |
frameshift variant |
-/T
|
delins
|
1.6E-05;
4.0E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
2 |
2007 |
2009 |
rs773019082
|
1.000 |
0.120 |
4 |
5798585 |
splice acceptor variant |
G/A
|
snv
|
1.2E-05
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs121908424
|
1.000 |
0.120 |
4 |
5808274 |
stop gained |
C/T
|
snv
|
1.2E-05
|
2.1E-05
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs1424976594
|
1.000 |
0.120 |
4 |
5810453 |
splice region variant |
A/G
|
snv
|
8.5E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
2 |
2013 |
2017 |
rs1017946059
|
0.925 |
0.160 |
4 |
5731657 |
missense variant |
G/A
|
snv
|
8.1E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.800 |
1.000 |
2 |
2010 |
2013 |
rs753317536
|
0.790 |
0.160 |
4 |
5719239 |
intron variant |
G/A;C
|
snv
|
8.0E-06;
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs794726665
|
0.925 |
0.120 |
4 |
5793722 |
splice region variant |
G/A;T
|
snv
|
6.5E-06;
6.5E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
3 |
2000 |
2013 |
rs909612975
|
1.000 |
0.120 |
4 |
5793606 |
splice acceptor variant |
A/G
|
snv
|
6.4E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs1373632260
|
1.000 |
0.120 |
4 |
5793699 |
missense variant |
T/C
|
snv
|
6.4E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs1262933856
|
1.000 |
0.120 |
4 |
5793607 |
splice acceptor variant |
G/A
|
snv
|
6.4E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1446547358
|
0.925 |
0.160 |
4 |
5798724 |
stop gained |
C/T
|
snv
|
4.1E-06
|
1.4E-05
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs150814290
|
1.000 |
0.120 |
4 |
5745203 |
splice acceptor variant |
G/C
|
snv
|
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs896581899
|
1.000 |
0.120 |
4 |
5810377 |
stop gained |
C/T
|
snv
|
4.0E-06
|
7.0E-06
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs1007534611
|
1.000 |
0.120 |
4 |
5809612 |
splice donor variant |
G/T
|
snv
|
4.0E-06
|
2.1E-05
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs764397417
|
1.000 |
0.120 |
4 |
5783666 |
stop gained |
G/T
|
snv
|
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs751772225
|
1.000 |
0.120 |
4 |
5783672 |
stop gained |
C/T
|
snv
|
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs765269619
|
1.000 |
0.120 |
4 |
5783656 |
stop gained |
C/G;T
|
snv
|
4.0E-06;
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
|
0 |
|
|
rs760607210
|
1.000 |
0.120 |
4 |
5753840 |
frameshift variant |
G/-
|
delins
|
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs748523193
|
0.925 |
0.120 |
4 |
5729369 |
stop gained |
C/A;T
|
snv
|
4.0E-06;
4.0E-06
|
|
Ellis-Van Creveld Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
0.700 |
1.000 |
1 |
2009 |
2009 |