List of variants in gene PDGFRA reported as likely pathogenic for immune system cancer

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_006206.6(PDGFRA):c.1432T>C (p.Ser478Pro)	rs35597368	0.15258
NM_006206.6(PDGFRA):c.167G>C (p.Ser56Thr)	rs587778601

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