ClinVar Miner

Submissions for variant NM_024996.7(GFM1):c.1080G>A (p.Leu360=)

dbSNP: rs1722595341
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 RCV002796305 SCV003201901 likely benign not provided 2022-05-11 criteria provided, single submitter clinical testing

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