ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.843G>A (p.Leu281=)

dbSNP: rs1555064274
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001578778 SCV001806082 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578779 SCV001806083 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578780 SCV001806084 uncertain significance Usher syndrome type 1 2021-07-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002570816 SCV003225155 likely benign not provided 2022-08-19 criteria provided, single submitter clinical testing

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