Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs367784906
rs367784906
GRXCR1
CUI: C1414017
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 25
DEAFNESS, AUTOSOMAL RECESSIVE 25 		0.700 GeneticVariation UNIPROT Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. 20137778

2010
dbSNP: rs367784906
rs367784906
GRXCR1
CUI: C1414017
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 25
DEAFNESS, AUTOSOMAL RECESSIVE 25 		0.700 GeneticVariation UNIPROT Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. 20137774

2010