ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.3067-10C>T

gnomAD frequency: 0.00001  dbSNP: rs375115645
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897352 SCV001041493 benign not provided 2018-02-08 criteria provided, single submitter clinical testing

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