ClinVar Miner

Submissions for variant NM_001288705.3(CSF1R):c.1711T>G (p.Tyr571Asp)

dbSNP: rs1057519802
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000430977 SCV000505201 likely pathogenic Hematologic neoplasm 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440400 SCV000505202 likely pathogenic Myeloproliferative disorder 2016-05-13 no assertion criteria provided literature only

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