ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.66_71del (p.Gly23_Glu24del) (rs267606567)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005167 SCV000025344 pathogenic Somatotroph adenoma 2007-03-06 no assertion criteria provided literature only
GeneReviews RCV000005167 SCV000055841 probable-pathogenic Somatotroph adenoma 2012-06-21 no assertion criteria provided curation Converted during submission to Likely pathogenic.

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