ClinVar Miner

Submissions for variant NM_020469.2(ABO):c.261delG (p.Thr88Profs)

dbSNP: rs1556058284
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000948180 SCV001094378 benign not provided 2019-12-19 criteria provided, single submitter clinical testing
OMIM RCV000019309 SCV000039598 affects ABO blood group system 1990-05-17 no assertion criteria provided literature only

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