ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.543del (p.Ile182fs)

dbSNP: rs267606559
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005169 SCV000025346 pathogenic Somatotroph adenoma 2007-03-06 no assertion criteria provided literature only
GeneReviews RCV000005169 SCV000055839 not provided Somatotroph adenoma no assertion provided literature only

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