ClinVar Miner

Submissions for variant NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) (rs72470545)

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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 RCV000272950 SCV000432114 likely benign Parkinson Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000004589 SCV000024763 risk factor Parkinson disease 13 2008-07-01 no assertion criteria provided literature only

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