List of variants in gene combination LOC126860802, ZMYND11 reported as pathogenic by GeneDx

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.1317_1320del (p.Thr440fs)	rs1388355040
NM_001370100.5(ZMYND11):c.1328_1332del (p.Leu443fs)	rs2131964527
NM_001370100.5(ZMYND11):c.1652dup (p.Gln552fs)	rs1554793896

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