ClinVar Miner

Submissions for variant NM_001145026.2(PTPRQ):c.1187-27dup

dbSNP: rs56351124
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714158 SCV001941334 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001794500 SCV002033312 benign Hearing loss, autosomal dominant 73 2021-11-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001794499 SCV002033313 benign Autosomal recessive nonsyndromic hearing loss 84A 2021-11-07 criteria provided, single submitter clinical testing

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