ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.2267T>A (p.Val756Glu)

dbSNP: rs1777894570
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV001289473 SCV001477307 uncertain significance Hearing impairment 2020-10-28 criteria provided, single submitter clinical testing

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