ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.2718T>C (p.Asp906=)

gnomAD frequency: 0.00001  dbSNP: rs1456578169
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 RCV001402453 SCV001604303 likely benign 46,XY sex reversal 9 2018-10-22 criteria provided, single submitter clinical testing

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