ClinVar Miner

List of variants in gene MPL reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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.1609C>T (p.Arg537Trp)	rs148784027	0.00003
NM_005373.3(MPL):c.1781T>G (p.Leu594Trp)	rs1448812001

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