ClinVar Miner

Submissions for variant NM_001303052.2(MYT1L):c.3255T>C (p.Asp1085=)

gnomAD frequency: 0.04144  dbSNP: rs2288179
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 RCV001695955 SCV001912299 benign not provided 2018-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001695955 SCV005283736 benign not provided criteria provided, single submitter not provided

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