ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.*10A>C

gnomAD frequency: 0.00375  dbSNP: rs200994158
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000404521 SCV000416439 uncertain significance Congenital lactase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000309257 SCV000416440 uncertain significance Lactose intolerance 2016-06-14 criteria provided, single submitter clinical testing

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