List of variants in gene LYST reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.574T>G (p.Leu192Val)	rs7524261	0.04386
NM_000081.4(LYST):c.8411G>A (p.Gly2804Asp)	rs35333195	0.04044
NM_000081.4(LYST):c.3989A>C (p.Asp1330Ala)	rs74641549	0.04030
NM_000081.4(LYST):c.3050G>A (p.Ser1017Asn)	rs10465613	0.03661
NM_000081.4(LYST):c.7137A>C (p.Leu2379=)	rs61738992	0.02884
NM_000081.4(LYST):c.11268-5del	rs36014994

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