ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.156_160del (p.His52fs)

dbSNP: rs1881779084
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001095652 SCV001251407 likely pathogenic Rett syndrome, congenital variant 2019-10-08 criteria provided, single submitter clinical testing

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