List of variants in gene combination LOC126860802, ZMYND11 reported as uncertain significance by Revvity Omics, Revvity

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1370C>T (p.Thr457Ile)	rs1053967935	0.00002
NM_001370100.5(ZMYND11):c.1273C>T (p.Pro425Ser)	rs1204710018	0.00001

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