ClinVar Miner

Submissions for variant NM_006261.5(PROP1):c.109+435G>A

gnomAD frequency: 0.06917  dbSNP: rs73346254
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 RCV001523529 SCV001733246 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836440 SCV002081871 benign Pituitary hormone deficiency, combined, 2 2019-12-30 no assertion criteria provided clinical testing

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