ClinVar Miner

List of variants in gene MPL reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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.1719G>C (p.Lys573Asn)	rs774393112	0.00001
NM_005373.3(MPL):c.1589C>T (p.Pro530Leu)	rs775704066

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