ClinVar Miner

List of variants in gene MPL reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.1336G>A (p.Gly446Arg)	rs561818288	0.00046
NM_005373.3(MPL):c.313T>C (p.Phe105Leu)	rs145313814	0.00010

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