ClinVar Miner

List of variants reported as uncertain significance for Plasminogen deficiency, type I

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Total variants: 5

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HGVS	dbSNP
NM_000301.3(PLG):c.1217C>A (p.Pro406Gln)
NM_000301.3(PLG):c.1469G>A (p.Arg490Gln)	rs140537724
NM_000301.3(PLG):c.1858G>A (p.Ala620Thr)	rs121918027
NM_000301.3(PLG):c.2278A>G (p.Ser760Gly)
NM_000301.3(PLG):c.950+4A>G

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