ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.945G>A (p.Pro315=)

dbSNP: rs150450873
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000941373 SCV001087258 likely benign not provided 2024-01-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578791 SCV001806101 likely benign Autosomal recessive nonsyndromic hearing loss 23 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578792 SCV001806102 likely benign Usher syndrome type 1F 2021-07-14 criteria provided, single submitter clinical testing

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