ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.9486G>C (p.Gln3162His)

dbSNP: rs1568524894
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000721740 SCV000852871 uncertain significance not provided 2018-09-04 criteria provided, single submitter clinical testing

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