ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.314G>C (p.Arg105Thr)

dbSNP: rs33911434
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507183 SCV000603931 likely benign not specified 2016-11-08 criteria provided, single submitter clinical testing
OMIM RCV000016597 SCV000036866 other HEMOGLOBIN SHERWOOD FOREST 2017-12-12 no assertion criteria provided literature only

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