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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.1565+5C>T	rs41269541	0.00488
NM_005373.3(MPL):c.1654-10T>A	rs200460456	0.00196
NM_005373.3(MPL):c.754T>C (p.Tyr252His)	rs141311765	0.00124
NM_005373.3(MPL):c.1488C>T (p.Thr496=)	rs140091584	0.00056
NM_005373.3(MPL):c.1336G>A (p.Gly446Arg)	rs561818288	0.00049
NM_005373.3(MPL):c.1102G>T (p.Val368Leu)	rs149810307	0.00039
NM_005373.3(MPL):c.549G>A (p.Thr183=)	rs147130173	0.00024
NM_005373.3(MPL):c.1666G>T (p.Val556Phe)	rs150004498	0.00023
NM_005373.3(MPL):c.209C>T (p.Pro70Leu)	rs61754776	0.00021
NM_005373.3(MPL):c.1467C>T (p.Thr489=)	rs759161511	0.00009
NM_005373.3(MPL):c.1063A>G (p.Lys355Glu)	rs546510242

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