ClinVar Miner

List of variants in gene combination LOC126860802, ZMYND11 reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1390_1391insCC (p.Gln464fs)	rs2540044081
NM_001370100.5(ZMYND11):c.1581dup (p.Cys528fs)	rs2131978117
NM_001370100.5(ZMYND11):c.1685G>C (p.Trp562Ser)	rs2131979217

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