ClinVar Miner

Submissions for variant NM_000173.7(GP1BA):c.413G>T (p.Gly138Val)

dbSNP: rs1970365829
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Birmingham Platelet Group; University of Birmingham RCV001270613 SCV001450912 likely pathogenic Abnormal bleeding; Thrombocytopenia 2020-05-01 no assertion criteria provided research

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