rs367826984

This variant is located in the GRXCR2 gene.

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ClinVar annotation

Uncertain Significance★★★☆
3 submitters2 publications

not provided; Autosomal recessive nonsyndromic hearing loss 101; not specified

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About GRXCR2

This gene encodes a protein containing a glutaredoxin domain, which functions in protein S-glutathionylation. A mutation in this gene was found in a family with autoosomal recessive nonsyndromic sensorineural deafness-101. [provided by RefSeq, Jun 2014]

View all GRXCR2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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