ClinVar Miner

Submissions for variant NM_001567.4(INPPL1):c.1091-25A>G

gnomAD frequency: 0.32600  dbSNP: rs2276047
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714037 SCV001941107 benign not provided 2018-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730987 SCV001981290 benign Opsismodysplasia 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001714037 SCV005235931 benign not provided criteria provided, single submitter not provided

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