ClinVar Miner

Submissions for variant NM_020066.5(FMN2):c.1378G>A (p.Ala460Thr)

dbSNP: rs1463766241
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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 RCV000790947 SCV000930201 uncertain significance Intellectual disability, autosomal recessive 47 2019-04-27 criteria provided, single submitter clinical testing

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