List of variants in gene MPL reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.1102G>T (p.Val368Leu)	rs149810307	0.00039
NM_005373.3(MPL):c.549G>A (p.Thr183=)	rs147130173	0.00023
NM_005373.3(MPL):c.173C>T (p.Ala58Val)	rs6087	0.00005
NM_005373.3(MPL):c.584_585delinsGG (p.Pro195Arg)	rs2153916807
NM_005373.3(MPL):c.869A>C (p.Gln290Pro)

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