ClinVar Miner

List of variants reported as uncertain significance for not specified by Center for Human Genetics, University of Leuven

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005120.3(MED12):c.1562G>A (p.Arg521His)	rs875989806	0.00001
NG_012570.1:g.7766_7770delTAGGTinsAA	rs875989809
NM_018486.3(HDAC8):c.958G>A (p.Gly320Arg)	rs398122909

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