ClinVar Miner

Submissions for variant NM_001368397.1(FRMPD4):c.580G>A (p.Val194Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV001170006 SCV001251926 uncertain significance Mental retardation, X-linked 104 2020-05-03 criteria provided, single submitter clinical testing

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