ClinVar Miner

Submissions for variant NM_014263.4(YME1L1):c.33+24T>A

gnomAD frequency: 0.07350  dbSNP: rs2274637
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654470 SCV001864695 benign not provided 2021-05-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001654470 SCV005316345 benign not provided criteria provided, single submitter not provided

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