ClinVar Miner

Submissions for variant NM_198506.5(LRIT3):c.1467C>T (p.Asn489=)

gnomAD frequency: 0.00004  dbSNP: rs369821286
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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
Eurofins Ntd Llc (ga) RCV000314165 SCV000343142 uncertain significance not provided 2016-07-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000314165 SCV001651913 likely benign not provided 2024-06-21 criteria provided, single submitter clinical testing

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