rs121912585
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121912586
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121912587
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121912588
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121912589
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121912590
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs864321718
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121912585
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.
|
24715754 |
2014 |
rs121912585
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
|
14595441 |
2003 |
rs121912585
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
|
16157808 |
2005 |
rs121912585
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
|
17511870 |
2007 |
rs121912586
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
|
17511870 |
2007 |
rs121912586
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
|
14595441 |
2003 |
rs121912586
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
|
16157808 |
2005 |
rs121912586
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.
|
24715754 |
2014 |
rs121912587
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.
|
24715754 |
2014 |
rs121912587
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
|
16157808 |
2005 |
rs121912587
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
|
14595441 |
2003 |
rs121912587
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
|
17511870 |
2007 |
rs121912588
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.
|
24715754 |
2014 |
rs121912588
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
|
16157808 |
2005 |
rs121912588
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
|
14595441 |
2003 |
rs121912588
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
|
17511870 |
2007 |
rs121912589
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
|
14595441 |
2003 |
rs121912589
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
|
17511870 |
2007 |