List of variants in gene MPL reported as uncertain significance for Primary myelofibrosis; Thrombocythemia 2; Congenital amegakaryocytic thrombocytopenia 1

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.173C>T (p.Ala58Val)	rs6087	0.00005
NM_005373.3(MPL):c.409A>G (p.Ser137Gly)
NM_005373.3(MPL):c.869A>C (p.Gln290Pro)
NM_005373.3(MPL):c.933_935dup (p.Ser311_Gln312insHis)

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