List of variants in gene LYST reported as likely benign by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.5518T>G (p.Ser1840Ala)	rs115330112	0.00485
NM_000081.4(LYST):c.6482A>C (p.Glu2161Ala)	rs147756847	0.00421
NM_000081.4(LYST):c.8913T>G (p.Asn2971Lys)	rs34702903	0.00276
NM_000081.4(LYST):c.2946T>C (p.Tyr982=)	rs145892183	0.00034

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