ClinVar Miner

Submissions for variant NM_000518.4(HBB):c.34G>T (p.Val12Phe)

dbSNP: rs33974228
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759071 SCV000888156 uncertain significance not provided 2018-05-24 criteria provided, single submitter clinical testing
OMIM RCV000016800 SCV000037070 other HEMOGLOBIN WASHTENAW 2017-12-12 no assertion criteria provided literature only

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