List of variants in gene combination LOC126859861, PLG reported as pathogenic for hematologic disorder

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_000301.5(PLG):c.1858G>A (p.Ala620Thr)	rs121918027	0.00036
NM_000301.5(PLG):c.1848G>A (p.Trp616Ter)	rs121918031

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