List of variants in gene combination LOC126860802, ZMYND11 reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1273C>T (p.Pro425Ser)	rs1204710018	0.00001
NM_001370100.5(ZMYND11):c.1282C>T (p.Pro428Ser)	rs1554793294	0.00001
NM_001370100.5(ZMYND11):c.1363A>G (p.Thr455Ala)	rs1554793377	0.00001
NM_001370100.5(ZMYND11):c.1252G>T (p.Val418Leu)
NM_001370100.5(ZMYND11):c.1259C>A (p.Ser420Tyr)	rs1554793259
NM_001370100.5(ZMYND11):c.1296A>C (p.Glu432Asp)
NM_001370100.5(ZMYND11):c.1331G>A (p.Ser444Asn)
NM_001370100.5(ZMYND11):c.1340C>T (p.Ser447Leu)	rs1554793325
NM_001370100.5(ZMYND11):c.1475G>T (p.Arg492Leu)	rs751729106
NM_001370100.5(ZMYND11):c.1477G>C (p.Val493Leu)	rs950513406
NM_001370100.5(ZMYND11):c.1516GAA[2] (p.Glu508del)	rs2131976871
NM_001370100.5(ZMYND11):c.1672AAG[2] (p.Lys560del)

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