Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912585
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

dbSNP: rs121912586
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

dbSNP: rs121912587
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

dbSNP: rs121912588
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

dbSNP: rs121912589
rs121912589
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

dbSNP: rs121912590
rs121912590
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

dbSNP: rs121912585
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

dbSNP: rs121912586
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

dbSNP: rs121912587
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

dbSNP: rs121912588
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

dbSNP: rs121912589
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

dbSNP: rs121912590
rs121912590
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

dbSNP: rs121912585
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

dbSNP: rs121912586
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

dbSNP: rs121912587
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

dbSNP: rs121912588
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

dbSNP: rs121912589
rs121912589
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

dbSNP: rs121912590
rs121912590
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

dbSNP: rs121912585
rs121912585
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912586
rs121912586
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912587
rs121912587
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912588
rs121912588
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912589
rs121912589
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912590
rs121912590
0.800 GeneticVariation UNIPROT Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 14595441

2003

dbSNP: rs121912585
rs121912585
A 0.800 CausalMutation CLINVAR