OTOGL, otogelin like, 283310

N. diseases: 9; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1233562246
rs1233562246
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C3554159
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 84B
G 0.700 CausalMutation CLINVAR
dbSNP: rs1477766714
rs1477766714
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C3554159
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 84B
G 0.700 GeneticVariation CLINVAR
dbSNP: rs397514588
rs397514588
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C3554159
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 84B
T 0.700 CausalMutation CLINVAR
dbSNP: rs902734999
rs902734999
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C3554159
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 84B
A 0.700 CausalMutation CLINVAR
dbSNP: rs952235302
rs952235302
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C3554159
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 84B
A 0.700 CausalMutation CLINVAR