ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.2083G>A (p.Ala695Thr)

dbSNP: rs1954489249
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001329738 SCV001521258 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2019-12-10 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Revvity Omics, Revvity Omics RCV003132422 SCV003817841 uncertain significance not provided 2023-08-08 criteria provided, single submitter clinical testing

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