ClinVar Miner

Submissions for variant NM_153002.3(GPR156):c.1863dup (p.His622fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mustafa Tekin Lab, University Of Miami, Miller School Of Medicine RCV003447652 SCV004022366 likely pathogenic Hearing loss, autosomal recessive 2023-05-24 no assertion criteria provided research
OMIM RCV003387447 SCV004098890 pathogenic Hearing loss, autosomal recessive 121 2023-10-26 no assertion criteria provided literature only

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