List of variants in gene PROS1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.-62T>G	rs556711298	0.00299
NM_000313.4(PROS1):c.76+7A>G	rs201928951	0.00056
NM_000313.4(PROS1):c.284G>A (p.Gly95Glu)	rs144526169	0.00040
NM_000313.4(PROS1):c.1324-3T>G	rs200270949	0.00005
NM_000313.4(PROS1):c.1465G>A (p.Gly489Arg)	rs762438750	0.00001
NM_000313.4(PROS1):c.1832T>C (p.Met611Thr)	rs750531364	0.00001
NM_000313.4(PROS1):c.469+5G>A	rs756682607	0.00001
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu)	rs7614835
NM_000313.4(PROS1):c.1420C>T (p.His474Tyr)	rs1468370376
NM_000313.4(PROS1):c.24C>G (p.Cys8Trp)	rs2471855615
NM_000313.4(PROS1):c.338G>T (p.Cys113Phe)
NM_000313.4(PROS1):c.56T>G (p.Leu19Arg)
NM_000313.4(PROS1):c.6G>T (p.Arg2Ser)
NM_000313.4(PROS1):c.849G>A (p.Glu283=)	rs767767470
NM_000313.4(PROS1):c.965+5G>A	rs1559932716

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