ClinVar Miner

Submissions for variant NM_001376232.1(ZP2):c.151+1G>A

dbSNP: rs772233041
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory Cellgenetics, GMDL Cellgenetics RCV002467398 SCV002762670 likely pathogenic Oocyte maturation defect 6 2022-04-01 criteria provided, single submitter clinical testing The variant ZP2:c.151+1G>A was classified as Likely pathogenic. The classification was assigned based on the following ACMG criteria: PVS1, PM2.

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