List of variants in gene combination C10orf55, LOC126860960, PLAU reported as uncertain significance 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.368+6G>C	rs186447765	0.00003
NM_002658.6(PLAU):c.316G>C (p.Ala106Pro)	rs886047206
NM_002658.6(PLAU):c.467dup (p.Pro157fs)	rs1435611170
NM_002658.6(PLAU):c.539T>C (p.Ile180Thr)
NM_002658.6(PLAU):c.548A>G (p.Glu183Gly)
NM_002658.6(PLAU):c.581C>A (p.Ala194Glu)	rs145865648
NM_002658.6(PLAU):c.735C>A (p.Asn245Lys)	rs1249124159
NM_002658.6(PLAU):c.750G>C (p.Gly250=)	rs886047207
NM_002658.6(PLAU):c.754A>T (p.Met252Leu)

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