List of variants in gene LYZ reported as likely benign for amyloidosis

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000239.3(LYZ):c.263C>A (p.Thr88Asn)	rs1800973	0.04360
NM_000239.3(LYZ):c.156G>A (p.Trp52Ter)	rs764263034	0.00004
NM_000239.3(LYZ):c.434G>A (p.Gly145Asp)	rs762616173	0.00004
NM_000239.3(LYZ):c.272C>G (p.Ala91Gly)	rs776898103	0.00003
NM_000239.3(LYZ):c.*735del	rs148802204
NM_000239.3(LYZ):c.239G>A (p.Arg80His)
NM_000239.3(LYZ):c.398G>A (p.Arg133His)
NM_000239.3(LYZ):c.40G>T (p.Val14Phe)

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