ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.3369A>G (p.Leu1123=)

gnomAD frequency: 0.01580  dbSNP: rs16873744
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000469703 SCV000557291 benign 46,XY sex reversal 9 2024-01-29 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230508 SCV003928348 benign not specified 2023-04-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004712860 SCV005267909 benign not provided criteria provided, single submitter not provided

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