Variants in gene MPL with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.340G>A (p.Val114Met)	rs12731981	0.02191
NM_005373.3(MPL):c.117G>T (p.Lys39Asn)	rs17292650	0.01420
NM_005373.3(MPL):c.543T>C (p.Gly181=)	rs17572791	0.00819
NM_005373.3(MPL):c.1309-10C>T	rs139486615	0.00602
NM_005373.3(MPL):c.1565+5C>T	rs41269541	0.00488
NM_005373.3(MPL):c.210G>A (p.Pro70=)	rs6086	0.00482
NM_005373.3(MPL):c.391+47C>T	rs839994	0.00367
NM_005373.3(MPL):c.1654-10T>A	rs200460456	0.00196

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