ClinVar Miner

Submissions for variant NM_004407.4(DMP1):c.102+79A>G

gnomAD frequency: 0.78191  dbSNP: rs2615479
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 RCV001611788 SCV001837190 benign not provided 2018-08-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001611788 SCV005303291 benign not provided criteria provided, single submitter not provided

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