List of variants in gene LYZ reported as 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000239.3(LYZ):c.*178C>T	rs710794	0.89111
NM_000239.3(LYZ):c.*835C>T	rs1384	0.40016
NM_000239.3(LYZ):c.*655G>T	rs8612	0.10799
NM_000239.3(LYZ):c.-1C>T	rs513342	0.06603
NM_000239.3(LYZ):c.263C>A (p.Thr88Asn)	rs1800973	0.04360
NM_000239.3(LYZ):c.*461G>A	rs531233279	0.00770
NM_000239.3(LYZ):c.10C>G (p.Leu4Val)	rs58131341	0.00302
NM_000239.3(LYZ):c.*890T>C	rs188271229	0.00204
NM_000239.3(LYZ):c.*418C>A	rs534565279	0.00177
NM_000239.3(LYZ):c.*415G>A	rs183441118	0.00159
NM_000239.3(LYZ):c.*413G>T	rs193040437	0.00128
NM_000239.3(LYZ):c.*169G>A	rs568058282	0.00126
NM_000239.3(LYZ):c.*191A>G	rs183375295	0.00101
NM_000239.3(LYZ):c.151A>T (p.Lys51Ter)	rs367682582	0.00002
NM_000239.3(LYZ):c.*266G>A	rs188313797
NM_000239.3(LYZ):c.*521G>A	rs567541896
NM_000239.3(LYZ):c.415G>C (p.Val139Leu)	rs367623154

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