List of variants in gene MPL reported as benign by GeneDx

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.981-41G>A	rs1760670	0.31103
NC_000001.11:g.43337551G>A	rs710252	0.30324
NM_005373.3(MPL):c.1469-70T>C	rs839995	0.29954
NM_005373.3(MPL):c.392-274G>T	rs77612379	0.05125
NM_005373.3(MPL):c.690A>G (p.Glu230=)	rs16830693	0.05049
NC_000001.11:g.43354522G>A	rs79064184	0.03603
NM_005373.3(MPL):c.691-178C>T	rs79089983	0.02540
NM_005373.3(MPL):c.340G>A (p.Val114Met)	rs12731981	0.02191
NM_005373.3(MPL):c.117G>T (p.Lys39Asn)	rs17292650	0.01329
NM_005373.3(MPL):c.1309-61T>C	rs111245827	0.01021
NM_005373.3(MPL):c.1565+5C>T	rs41269541	0.00488
NM_005373.3(MPL):c.210G>A (p.Pro70=)	rs6086	0.00452
NM_005373.3(MPL):c.391+47C>T	rs839994	0.00367
NM_005373.3(MPL):c.962G>A (p.Arg321Gln)	rs149265851	0.00072
NM_005373.3(MPL):c.1309-28C>G	rs573364731	0.00041

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