ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.3532C>T (p.Leu1178=)

dbSNP: rs886054864
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000285773 SCV000416491 uncertain significance Congenital lactase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343179 SCV000416492 uncertain significance Lactose intolerance 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002521289 SCV003018775 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing

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