ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.3908C>T (p.Thr1303Ile)

dbSNP: rs1746764895
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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 Statistical Genetics, Columbia University RCV001261383 SCV001438293 likely pathogenic Intellectual disability 2020-10-16 criteria provided, single submitter research

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