ClinVar Miner

Submissions for variant NM_000316.3(PTH1R):c.463G>T (p.Glu155Ter)

dbSNP: rs121434605
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014761 SCV000035016 pathogenic Primary failure of tooth eruption 2008-12-01 no assertion criteria provided literature only

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