List of variants in gene ZMYND11 reported as likely 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1776G>A (p.Ala592=)	rs770351439	0.00005
NM_001370100.5(ZMYND11):c.517-11C>T
NM_001370100.5(ZMYND11):c.612A>G (p.Lys204=)	rs1554788945

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