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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000301.5(PLG):c.112A>G (p.Lys38Glu)	rs73015965	0.00282
NM_000301.5(PLG):c.1469G>A (p.Arg490Gln)	rs140537724	0.00140
NM_000301.5(PLG):c.2045T>A (p.Ile682Asn)	rs147175166	0.00073
NM_000301.5(PLG):c.2263A>G (p.Ser755Gly)	rs1778416234	0.00001
NM_000301.5(PLG):c.86A>C (p.Gln29Pro)	rs1051644668	0.00001
NM_000301.5(PLG):c.1217C>A (p.Pro406Gln)	rs1582940083
NM_000301.5(PLG):c.2278A>G (p.Ser760Gly)	rs1582955692
NM_000301.5(PLG):c.266G>C (p.Arg89Thr)	rs143079629
NM_000301.5(PLG):c.466G>A (p.Asp156Asn)	rs756533019
NM_000301.5(PLG):c.950+4A>G	rs1582937995

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