List of variants in gene MYC reported as likely pathogenic for hematologic disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002467.6(MYC):c.173C>T (p.Pro58Leu)	rs1057519918
NM_002467.6(MYC):c.217A>C (p.Thr73Pro)	rs750664148
NM_002467.6(MYC):c.218C>T (p.Thr73Ile)	rs756091827

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