ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.1227G>T (p.Gln409His)

gnomAD frequency: 0.00097  dbSNP: rs201439692
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
Invitae RCV000655311 SCV000777241 likely benign 46,XY sex reversal 9 2023-12-02 criteria provided, single submitter clinical testing

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