List of variants in gene GLDC reported as likely benign by PreventionGenetics, part of Exact Sciences

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_000170.3(GLDC):c.2683A>G (p.Met895Val)	rs141152043	0.00200
NM_000170.3(GLDC):c.40C>A (p.Arg14Ser)	rs182760732	0.00197
NM_000170.3(GLDC):c.2955G>A (p.Thr985=)	rs142004524	0.00131
NM_000170.3(GLDC):c.1618A>C (p.Lys540Gln)	rs140516872	0.00127
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.2097C>T (p.Tyr699=)	rs149694787	0.00021
NM_000170.3(GLDC):c.2570-10T>C	rs373987254	0.00019
NM_000170.3(GLDC):c.1752T>C (p.Pro584=)	rs150647379	0.00012
NM_000170.3(GLDC):c.2028C>T (p.Ile676=)	rs372604935	0.00006
NM_000170.3(GLDC):c.2673C>T (p.His891=)	rs144939090	0.00004
NM_000170.3(GLDC):c.489A>G (p.Pro163=)	rs770044310	0.00004
NM_000170.3(GLDC):c.1917G>A (p.Gly639=)	rs776998782	0.00001
NM_000170.3(GLDC):c.861+10C>T	rs565335444	0.00001
NM_000170.3(GLDC):c.1035T>A (p.Pro345=)
NM_000170.3(GLDC):c.1893C>T (p.Ala631=)	rs565751857
NM_000170.3(GLDC):c.1908A>G (p.Lys636=)	rs552960907
NM_000170.3(GLDC):c.190G>T (p.Ala64Ser)	rs141601131

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