ClinVar Miner

List of variants in gene PTPRQ reported as not provided for Autosomal recessive nonsyndromic hearing loss 84A

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001145026.2(PTPRQ):c.715A>G (p.Arg239Gly)	rs281865414	0.00005
NM_001145026.2(PTPRQ):c.837T>A (p.Tyr279Ter)	rs183258549

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