List of variants in gene MPL reported as likely benign for Inborn genetic diseases

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.1570C>T (p.Leu524=)	rs146372205	0.00053
NM_005373.3(MPL):c.1841G>C (p.Gly614Ala)	rs138450235	0.00031
NM_005373.3(MPL):c.1640C>T (p.Ala547Val)	rs572129852	0.00003
NM_005373.3(MPL):c.916C>G (p.Gln306Glu)

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