ClinVar Miner

Submissions for variant NM_002299.4(LCT):c.4977-26T>C

gnomAD frequency: 0.03191  dbSNP: rs3213891
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595958 SCV001829156 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730861 SCV001981325 benign Congenital lactase deficiency 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001595958 SCV005245308 benign not provided criteria provided, single submitter not provided

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