ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.285C>T (p.Asp95=)

gnomAD frequency: 0.00014  dbSNP: rs371910925
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 RCV000862684 SCV001003222 likely benign 46,XY sex reversal 9 2023-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705802 SCV005224035 likely benign not provided criteria provided, single submitter not provided

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