VIM, vimentin, 7431

N. diseases: 644; N. variants: 6
Disease: CATARACT 30 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917775
rs121917775
Entrez Id: 7431;100507347
Gene Symbol: VIM;VIM-AS1
VIM;VIM-AS1
CUI: C3805411
Disease:
CATARACT 30 		0.800 GeneticVariation UNIPROT Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype-Phenotype Correlations in 27 Chinese Han Families. 28450710 2017
dbSNP: rs121917775
rs121917775
Entrez Id: 7431;100507347
Gene Symbol: VIM;VIM-AS1
VIM;VIM-AS1
CUI: C3805411
Disease:
CATARACT 30 		0.800 GeneticVariation UNIPROT Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing. 26694549 2016
dbSNP: rs121917775
rs121917775
Entrez Id: 7431;100507347
Gene Symbol: VIM;VIM-AS1
VIM;VIM-AS1
CUI: C3805411
Disease:
CATARACT 30 		0.800 GeneticVariation UNIPROT Dominant cataract formation in association with a vimentin assembly disrupting mutation. 19126778 2009
dbSNP: rs121917775
rs121917775
Entrez Id: 7431;100507347
Gene Symbol: VIM;VIM-AS1
VIM;VIM-AS1
CUI: C3805411
Disease:
CATARACT 30 		A 0.800 CausalMutation CLINVAR