ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.3438A>G (p.Ala1146=)

gnomAD frequency: 0.00006  dbSNP: rs369522665
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001407691 SCV001609668 likely benign 46,XY sex reversal 9 2023-11-02 criteria provided, single submitter clinical testing

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