ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.4122C>T (p.Tyr1374=) (rs557321611)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000301657 SCV000416477 uncertain significance Lactose intolerance 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000340089 SCV000416478 uncertain significance Congenital lactase deficiency 2016-06-14 criteria provided, single submitter clinical testing

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