List of variants in gene LYST reported as likely benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.5945C>T (p.Thr1982Ile)	rs146591126	0.00669
NM_000081.4(LYST):c.7059+7G>A	rs111764031	0.00582
NM_000081.4(LYST):c.6812A>G (p.Asp2271Gly)	rs112601869	0.00580
NM_000081.4(LYST):c.8898T>C (p.Tyr2966=)	rs144475533	0.00560
NM_000081.4(LYST):c.5518T>G (p.Ser1840Ala)	rs115330112	0.00485
NM_000081.4(LYST):c.-5C>T	rs141317482	0.00475
NM_000081.4(LYST):c.10800+4G>T	rs41308172	0.00441
NM_000081.4(LYST):c.1686G>C (p.Gln562His)	rs77091385	0.00394
NM_000081.4(LYST):c.5291G>C (p.Gly1764Ala)	rs35413645	0.00350
NM_000081.4(LYST):c.3359G>T (p.Ser1120Ile)	rs143223086	0.00302
NM_000081.4(LYST):c.7870C>T (p.Arg2624Trp)	rs150306354	0.00280
NM_000081.4(LYST):c.1384C>T (p.Pro462Ser)	rs77848653	0.00276
NM_000081.4(LYST):c.2363+4T>C	rs201398337	0.00252
NM_000081.4(LYST):c.6710A>C (p.Gln2237Pro)	rs138443479	0.00148
NM_000081.4(LYST):c.2769A>C (p.Ser923=)	rs112739986	0.00086
NM_000081.4(LYST):c.8027G>T (p.Ser2676Ile)	rs113209379	0.00086
NM_000081.4(LYST):c.7229+3A>G	rs529306869	0.00074
NM_000081.4(LYST):c.4863-4G>A	rs201382097	0.00032
NM_000081.4(LYST):c.368A>G (p.His123Arg)	rs3768067	0.00027
NM_000081.4(LYST):c.5374A>G (p.Asn1792Asp)	rs143696500	0.00010
NM_000081.4(LYST):c.2908A>C (p.Ile970Leu)	rs539146732	0.00001
NM_000081.4(LYST):c.11268-17dup	rs36014994

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