ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.*429A>C

gnomAD frequency: 0.01053  dbSNP: rs77631953
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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 RCV000322643 SCV000416429 likely benign Congenital lactase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000379568 SCV000416430 likely benign Lactose intolerance 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710844 SCV005262850 likely benign not provided criteria provided, single submitter not provided

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