Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565519673
rs1565519673
TECTA
CUI: C1384666
Disease: hearing impairment
hearing impairment 		CT 0.700 CausalMutation CLINVAR

dbSNP: rs1565536400
rs1565536400
TECTA
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1565541888
rs1565541888
TECTA
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs368050948
rs368050948
TECTA
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR