Tag

Hearing Loss

10 genetic variants with this tag.

RSID	Gene	Description	Category
rs80338939	GJB2 35delG	The most common cause of autosomal recessive nonsyndromic hearing loss in Eur...	Neurology & Cognition	Hearing Loss Sensorineural Congenital	Established
rs72474224	GJB2 V37I	Connexin 26 missense variant causing partial loss of cochlear gap junction fu...	Neurology & Cognition	Hearing Loss Sensorineural Congenital	Established
rs104894396	GJB2 W24X	Stop-gain mutation eliminating connexin 26 function; the most common GJB2 dea...	Neurology & Cognition	Hearing Loss Sensorineural Congenital	Established
rs80338942	GJB2 167delT	The most common GJB2 deafness allele in the Ashkenazi Jewish population (~4% ...	Neurology & Cognition	Hearing Loss Sensorineural Congenital	Established
rs35887543	GJB2 c.235delC	Frameshift deletion eliminating connexin 26 function; the most common GJB2 de...	Neurology & Cognition	Hearing Loss Sensorineural Congenital	Established
rs35887622	GJB2 M34T	Connexin 26 missense variant causing partial loss of cochlear gap junction fu...	Neurology & Cognition	Hearing Loss Sensorineural Carrier Status	Established
rs10421919	TMPRSS3	Near-gene variant tagging the TMPRSS3 hearing loss locus on chromosome 21, as...	Neurology & Cognition	Hearing Loss Sensorineural Carrier Status	Moderate
rs727503493	TMPRSS3 c.208delC (p.His70Thrfs*19)	Frameshift deletion in TMPRSS3 causing premature stop at codon 88; a severe p...	Neurology & Cognition	Hearing Loss Sensorineural Carrier Status	Strong
rs137853000	TMPRSS3 p.Arg216Leu (R216L)	Pathogenic missense variant at the TMPRSS3 autocatalytic cleavage site causin...	Neurology & Cognition	Hearing Loss Sensorineural Carrier Status	Strong
rs111033253	TMPRSS3 p.Ala306Thr (A306T)	Hypomorphic missense variant in the TMPRSS3 serine protease catalytic domain;...	Neurology & Cognition	Hearing Loss Sensorineural Carrier Status	Strong