ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.2430A>T (p.Pro810=)

gnomAD frequency: 0.00011  dbSNP: rs200002039
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001516080 SCV001724294 benign 46,XY sex reversal 9 2024-11-22 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821823 SCV002067087 likely benign not specified 2018-06-05 criteria provided, single submitter clinical testing

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