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

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1246_1247del (p.Glu416fs)	rs606231268
NM_001370100.5(ZMYND11):c.1262G>A (p.Ser421Asn)	rs869320713
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.1388_1389del (p.Cys463fs)	rs1952647904
NM_001370100.5(ZMYND11):c.1472_1473del (p.Glu491fs)	rs2540045854
NM_001370100.5(ZMYND11):c.1483C>T (p.Arg495Ter)	rs2540046247
NM_001370100.5(ZMYND11):c.1525_1526del (p.Lys509fs)	rs2131977010
NM_001370100.5(ZMYND11):c.1573dup (p.Asp525fs)	rs2540056456
NM_001370100.5(ZMYND11):c.1652dup (p.Gln552fs)	rs1554793896

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