ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.200-8T>G

gnomAD frequency: 0.00023  dbSNP: rs573002259
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002143450 SCV002453028 benign 46,XY sex reversal 9 2021-11-05 criteria provided, single submitter clinical testing

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