List of variants in gene combination C10orf55, LOC126860960, PLAU reported as benign for hematologic disorder

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002658.6(PLAU):c.681-7C>T	rs2227566	0.50640
NM_002658.6(PLAU):c.822C>T (p.Asn274=)	rs2227568	0.12381
NM_002658.6(PLAU):c.691A>C (p.Lys231Gln)	rs2227567	0.04766
NM_002658.6(PLAU):c.445C>T (p.His149Tyr)	rs117135013	0.00070
NM_002658.6(PLAU):c.581C>T (p.Ala194Val)	rs145865648	0.00011
NM_002658.6(PLAU):c.706A>G (p.Ile236Val)	rs150389556	0.00006
NM_002658.6(PLAU):c.308C>T (p.Thr103Met)	rs370278611	0.00004
NM_002658.6(PLAU):c.602G>T (p.Arg201Leu)	rs549461157	0.00001
NM_002658.6(PLAU):c.559A>G (p.Ile187Val)	rs528761202

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