ClinVar Miner

Submissions for variant NM_006261.5(PROP1):c.629dup (p.Pro211fs)

dbSNP: rs761018422
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673608 SCV000798832 uncertain significance Pituitary hormone deficiency, combined, 2 2018-03-26 criteria provided, single submitter clinical testing
Baylor Genetics RCV000673608 SCV004206543 likely pathogenic Pituitary hormone deficiency, combined, 2 2022-11-19 criteria provided, single submitter clinical testing

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