List of variants in gene PDGFRA reported as likely benign for immune system 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.368-3C>T	rs55947416	0.04647
NM_006206.6(PDGFRA):c.1122G>C (p.Arg374Ser)	rs61735622	0.00183
NM_006206.6(PDGFRA):c.*2100A>G	rs192159089	0.00083
NM_006206.5(PDGFRA):c.*2973+14G>A	rs137930765	0.00074
NM_006206.6(PDGFRA):c.1285G>A (p.Gly429Arg)	rs150577828	0.00034
NM_006206.6(PDGFRA):c.*1778C>A	rs182602738	0.00019
NM_006206.6(PDGFRA):c.1135T>G (p.Leu379Val)	rs199827643	0.00014
NM_006206.6(PDGFRA):c.17C>T (p.Pro6Leu)	rs754092062	0.00009
NM_006206.6(PDGFRA):c.896T>C (p.Val299Ala)	rs200033396	0.00006
NM_006206.6(PDGFRA):c.2897A>G (p.His966Arg)	rs200042995	0.00004
NM_006206.6(PDGFRA):c.*505A>G	rs373134586	0.00001
NM_006206.6(PDGFRA):c.1471G>A (p.Ala491Thr)	rs563016888	0.00001
NM_006206.6(PDGFRA):c.2266G>A (p.Asp756Asn)	rs555347387	0.00001
NM_006206.6(PDGFRA):c.3191A>G (p.Asp1064Gly)	rs375050626	0.00001
NM_006206.6(PDGFRA):c.853A>G (p.Ser285Gly)	rs541057765

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