ClinVar Miner

Submissions for variant NM_001032283.3(TMPO):c.183G>A (p.Gly61=)

gnomAD frequency: 0.00001  dbSNP: rs780119963
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001502395 SCV001707229 likely benign Loeys-Dietz syndrome 2 2023-08-27 criteria provided, single submitter clinical testing

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