List of variants in gene GLDC reported as benign by Invitae

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_000170.3(GLDC):c.501G>A (p.Glu167=)	rs35374927	0.22564
NM_000170.3(GLDC):c.249G>A (p.Gly83=)	rs12341698	0.21682
NM_000170.3(GLDC):c.660C>T (p.Leu220=)	rs2228095	0.07130
NM_000170.3(GLDC):c.438G>A (p.Thr146=)	rs13289273	0.06458
NM_000170.3(GLDC):c.1384C>G (p.Leu462Val)	rs73400312	0.04004
NM_000170.3(GLDC):c.666T>C (p.Asp222=)	rs12004164	0.02547
NM_000170.3(GLDC):c.1482+19T>C	rs79114789	0.02433
NM_000170.3(GLDC):c.671G>A (p.Arg224His)	rs28617412	0.02214
NM_000170.3(GLDC):c.1815C>T (p.Leu605=)	rs74461075	0.01328
NM_000170.3(GLDC):c.2203-19G>A	rs13440229	0.01223
NM_000170.3(GLDC):c.2380G>A (p.Ala794Thr)	rs141933811	0.00728
NM_000170.3(GLDC):c.319A>G (p.Met107Val)	rs138454333	0.00707
NM_000170.3(GLDC):c.52G>T (p.Gly18Cys)	rs535143891	0.00670
NM_000170.3(GLDC):c.2203G>T (p.Val735Leu)	rs143119940	0.00650
NM_000170.3(GLDC):c.2919+3A>G	rs73639325	0.00620
NM_000170.3(GLDC):c.871T>G (p.Cys291Gly)	rs141014950	0.00580
NM_000170.3(GLDC):c.1707+8G>A	rs144666843	0.00464
NM_000170.3(GLDC):c.1261+19T>C	rs192870343	0.00431
NM_000170.3(GLDC):c.2457+8C>T	rs147308839	0.00421
NM_000170.3(GLDC):c.1705G>A (p.Ala569Thr)	rs151268759	0.00419
NM_000170.3(GLDC):c.2113G>A (p.Val705Met)	rs147275962	0.00405
NM_000170.3(GLDC):c.678C>T (p.His226=)	rs12006003	0.00338
NM_000170.3(GLDC):c.2053-5C>G	rs140877566	0.00278
NM_000170.3(GLDC):c.1229G>A (p.Arg410Lys)	rs144090917	0.00234
NM_000170.3(GLDC):c.1156-7C>G	rs150095531	0.00208
NM_000170.3(GLDC):c.2748G>A (p.Leu916=)	rs139982267	0.00203
NM_000170.3(GLDC):c.1927-9A>G	rs41281773	0.00180
NM_000170.3(GLDC):c.2955G>A (p.Thr985=)	rs142004524	0.00131
NM_000170.3(GLDC):c.2988G>C (p.Gln996His)	rs138640017	0.00112
NM_000170.3(GLDC):c.498T>C (p.Pro166=)	rs150193069	0.00110
NM_000170.3(GLDC):c.222C>T (p.Asp74=)	rs148373517	0.00096
NM_000170.3(GLDC):c.2730G>A (p.Ser910=)	rs144937031	0.00061
NM_000170.3(GLDC):c.936C>T (p.Ile312=)	rs79057118	0.00058
NM_000170.3(GLDC):c.470+11T>C	rs142534180	0.00051
NM_000170.3(GLDC):c.2202+19C>T	rs187370615	0.00041
NM_000170.3(GLDC):c.124G>A (p.Gly42Arg)	rs190430477	0.00028
NM_000170.3(GLDC):c.1581-5C>T	rs184463452	0.00018
NM_000170.3(GLDC):c.635+16A>G	rs182471927	0.00012
NM_000170.3(GLDC):c.2920-8C>T	rs138786708	0.00006
NM_000170.3(GLDC):c.1508A>C (p.Glu503Ala)	rs201890453	0.00005
NM_000170.3(GLDC):c.250C>T (p.Leu84=)	rs746606221	0.00005
NM_000170.3(GLDC):c.63C>A (p.Arg21=)	rs372141443	0.00001
NM_000170.3(GLDC):c.861+10C>T	rs565335444	0.00001
NM_000170.3(GLDC):c.1545G>A (p.Arg515=)	rs121964976
NM_000170.3(GLDC):c.2316-13_2316-12dup	rs3215923
NM_000170.3(GLDC):c.2316-6del	rs3215923
NM_000170.3(GLDC):c.2316-6dup	rs3215923
NM_000170.3(GLDC):c.2490G>T (p.Thr830=)	rs145407593
NM_000170.3(GLDC):c.636-12del

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