ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.1776T>C (p.Pro592=)

gnomAD frequency: 0.05790  dbSNP: rs16873732
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243857 SCV000311825 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000475888 SCV000557289 benign 46,XY sex reversal 9 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001651198 SCV001870085 benign not provided 2018-12-26 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000243857 SCV004029061 benign not specified 2023-07-03 criteria provided, single submitter clinical testing

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