ClinVar Miner

Submissions for variant NM_015120.4(ALMS1):c.671C>A (p.Ser224Tyr) (rs886038615)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000363881 SCV000431904 likely benign Alstrom syndrome 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000241558 SCV000312403 benign not specified criteria provided, single submitter clinical testing

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