ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.6725C>T (p.Thr2242Met)

gnomAD frequency: 0.00001  dbSNP: rs55916212
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897498 SCV001041644 benign not provided 2018-02-13 criteria provided, single submitter clinical testing
New York Genome Center RCV000897498 SCV002564199 uncertain significance not provided 2021-09-26 criteria provided, single submitter clinical testing

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