List of variants in gene LYST reported as likely 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.10941-7C>A	rs72761794	0.00614
NM_000081.4(LYST):c.5518T>G (p.Ser1840Ala)	rs115330112	0.00485
NM_000081.4(LYST):c.10800+4G>T	rs41308172	0.00441
NM_000081.4(LYST):c.4548C>T (p.Ser1516=)	rs116551057	0.00108
NM_000081.4(LYST):c.7506A>G (p.Gln2502=)	rs140434436	0.00106
NM_000081.4(LYST):c.3507C>T (p.Leu1169=)	rs74861744	0.00083
NM_000081.4(LYST):c.2363+10dup	rs760632806	0.00058
NM_000081.4(LYST):c.143A>G (p.His48Arg)	rs200132460	0.00046
NM_000081.4(LYST):c.4006+8G>A	rs369153654	0.00021
NM_000081.4(LYST):c.6432A>G (p.Ser2144=)	rs145080654	0.00011
NM_000081.4(LYST):c.3030A>G (p.Gly1010=)	rs751511204	0.00006
NM_000081.4(LYST):c.9804A>G (p.Pro3268=)	rs368740409	0.00004
NM_000081.4(LYST):c.2757G>A (p.Ser919=)	rs753541871	0.00002
NM_000081.4(LYST):c.9834T>C (p.Thr3278=)	rs901343967	0.00002
NM_000081.4(LYST):c.5037T>C (p.Gly1679=)	rs753293453	0.00001
NM_000081.4(LYST):c.6216A>G (p.Val2072=)	rs371248013	0.00001
NM_000081.4(LYST):c.5922+10A>G	rs375422713
NM_000081.4(LYST):c.9785-21_9785-17del	rs547173744

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