List of variants in gene MPL reported as uncertain significance for Thrombocythemia 2

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.1610G>A (p.Arg537Gln)	rs3820551	0.00009
NM_005373.3(MPL):c.1169G>A (p.Arg390His)	rs1298113648	0.00001
NM_005373.3(MPL):c.1612G>C (p.Val538Leu)
NM_005373.3(MPL):c.1719G>C (p.Lys573Asn)
NM_005373.3(MPL):c.684T>A (p.Ser228Arg)

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