ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.1461G>A (p.Ala487=) (rs146206234)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000364638 SCV000416521 uncertain significance Congenital lactase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000406168 SCV000416522 uncertain significance Lactose intolerance 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV001519714 SCV001728633 benign not provided 2020-10-08 criteria provided, single submitter clinical testing

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