List of variants in gene PDGFRA reported as benign by Sema4, Sema4

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.368-3C>T	rs55947416	0.04647
NM_006206.6(PDGFRA):c.236G>A (p.Gly79Asp)	rs36035373	0.00897
NM_006206.6(PDGFRA):c.201C>T (p.Ser67=)	rs35805947	0.00429
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe)	rs139913632	0.00307
NM_006206.6(PDGFRA):c.1644T>C (p.Ile548=)	rs115085731	0.00246

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