ClinVar Miner

List of variants in gene PDGFRB reported as likely benign for Myeloproliferative disorder, chronic, with eosinophilia

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002609.4(PDGFRB):c.946G>A (p.Val316Met)	rs41287112	0.00287
NM_002609.4(PDGFRB):c.2523G>A (p.Lys841=)	rs41287108	0.00236

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