ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.167G>C (p.Ser56Thr)

dbSNP: rs587778601
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000533882 SCV000630571 likely benign Gastrointestinal stromal tumor 2024-01-19 criteria provided, single submitter clinical testing
Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology RCV002284190 SCV002573653 likely pathogenic Myeloproliferative neoplasm, unclassifiable 2022-08-25 criteria provided, single submitter clinical testing
ITMI RCV000121793 SCV000085991 not provided not specified 2013-09-19 no assertion provided reference population

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