CRYM, crystallin mu, 1428

N. diseases: 16; N. variants: 3
Disease: DEAFNESS, AUTOSOMAL DOMINANT 40 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894512
rs104894512
Entrez Id: 1428
Gene Symbol: CRYM
CRYM
CUI: C4084708
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 40 		0.800 GeneticVariation UNIPROT Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues. 12471561 2003
dbSNP: rs104894512
rs104894512
Entrez Id: 1428
Gene Symbol: CRYM
CRYM
CUI: C4084708
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 40 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894509
rs104894509
Entrez Id: 1428
Gene Symbol: CRYM
CRYM
CUI: C4084708
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 40 		A 0.700 CausalMutation CLINVAR