ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.532+28227T>C

gnomAD frequency: 0.51867  dbSNP: rs2218279
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 RCV002217908 SCV002379892 benign 46,XY sex reversal 9 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713135 SCV005267891 benign not provided criteria provided, single submitter not provided

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