List of variants in gene EZH2 reported as likely pathogenic for Lymphoma

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004456.5(EZH2):c.1936T>A (p.Tyr646Asn)	rs267601395
NM_004456.5(EZH2):c.1936T>C (p.Tyr646His)	rs267601395
NM_004456.5(EZH2):c.1937A>C (p.Tyr646Ser)	rs267601394
NM_004456.5(EZH2):c.1937A>T (p.Tyr646Phe)	rs267601394
NM_004456.5(EZH2):c.2045C>G (p.Ala682Gly)	rs1057519833

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