List of variants in gene EZH2 reported as benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004456.5(EZH2):c.553G>C (p.Asp185His)	rs2302427	0.05998
NM_004456.5(EZH2):c.2110+6T>G	rs41277434	0.04917
NM_004456.5(EZH2):c.1017T>C (p.Phe339=)	rs77051363	0.01331
NM_004456.5(EZH2):c.1731G>A (p.Pro577=)	rs41277437	0.01093
NM_004456.5(EZH2):c.2196-20T>C	rs116768205	0.01015
NM_004456.5(EZH2):c.485-7G>A	rs112932272	0.00984
NM_004456.5(EZH2):c.728+19G>C	rs114692729	0.00566
NM_004456.5(EZH2):c.2028T>C (p.Asn676=)	rs115842196	0.00457
NM_004456.5(EZH2):c.1240+9C>A	rs114320893	0.00121
NM_004456.5(EZH2):c.*21del	rs3217095
NM_004456.5(EZH2):c.118-4del	rs3214332
NM_004456.5(EZH2):c.2110+6T>C	rs41277434

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