List of variants in gene PDGFRB reported as benign for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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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.1391C>T (p.Thr464Met)	rs74943037	0.02595
NM_002609.4(PDGFRB):c.1854G>A (p.Thr618=)	rs56072663	0.02433
NM_002609.4(PDGFRB):c.1453G>A (p.Glu485Lys)	rs41287110	0.01976
NM_002609.4(PDGFRB):c.102C>T (p.Val34=)	rs17708515	0.00869
NM_002609.4(PDGFRB):c.1033C>T (p.Pro345Ser)	rs2229558	0.00834
NM_002609.4(PDGFRB):c.1149G>C (p.Leu383=)	rs2228439	0.00793
NM_002609.4(PDGFRB):c.365-4G>T	rs139448702	0.00583
NM_002609.4(PDGFRB):c.3119G>T (p.Gly1040Val)	rs149417689	0.00523

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