List of variants in gene PDGFRB reported as benign by PreventionGenetics, part of Exact Sciences

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002609.4(PDGFRB):c.3137+4A>G	rs246391	0.38064
NM_002609.4(PDGFRB):c.3252A>G (p.Pro1084=)	rs246388	0.36918
NM_002609.4(PDGFRB):c.2601A>G (p.Leu867=)	rs246395	0.26470
NM_002609.4(PDGFRB):c.3090C>T (p.Pro1030=)	rs2228440	0.09078
NM_002609.4(PDGFRB):c.85A>T (p.Ile29Phe)	rs17110944	0.07088
NM_002609.4(PDGFRB):c.102C>T (p.Val34=)	rs17708515	0.00869
NM_002609.4(PDGFRB):c.1149G>C (p.Leu383=)	rs2228439	0.00793
NM_002609.4(PDGFRB):c.590G>A (p.Arg197Lys)	rs116642123	0.00302
NM_002609.4(PDGFRB):c.486G>A (p.Glu162=)	rs147141808	0.00009

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