rs749906501

This variant is located in the GRHL2 gene.

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ClinVar annotation

Uncertain Significance
1 submitter1 publication

Progressive sensorineural hearing impairment

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About GRHL2

The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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