List of variants in gene GLUL reported as benign by Illumina Laboratory Services, Illumina

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_001033044.4(GLUL):c.*2118T>C	rs10458354	0.99979
NM_001033044.4(GLUL):c.*2307C>T	rs2296521	0.62516
NM_001033044.4(GLUL):c.*342T>A	rs9347	0.59226
NM_001033044.4(GLUL):c.*2644G>C	rs2296523	0.58857
NM_001033044.4(GLUL):c.195T>C (p.Ser65=)	rs1058111	0.58837
NM_001033044.4(GLUL):c.*919A>G	rs7734	0.58827
NM_001033044.4(GLUL):c.-14+1136G>T	rs4110992	0.01462
NM_001033044.4(GLUL):c.*1364G>A	rs115448180	0.01401
NM_001033044.4(GLUL):c.*1958G>A	rs79056692	0.01333
NM_001033044.4(GLUL):c.*1340C>A	rs78220577	0.01330
NM_001033044.4(GLUL):c.*547C>A	rs76673199	0.01330
NM_001033044.4(GLUL):c.825G>A (p.Glu275=)	rs35378126	0.01038
NM_001033044.4(GLUL):c.*1411C>T	rs1058806	0.00912
NM_001033044.4(GLUL):c.*966A>G	rs7543200	0.00834
NM_001033044.4(GLUL):c.*1276C>T	rs143904819	0.00400
NM_001033044.4(GLUL):c.768C>T (p.Phe256=)	rs6684136	0.00138
NM_001033044.4(GLUL):c.*2516A>G	rs140277335	0.00039
NM_001033044.4(GLUL):c.1909_1910insTCATTT	rs3028837
NM_001033044.4(GLUL):c.*1913A>T	rs4517308
NM_001033044.4(GLUL):c.*2631G>A	rs2296522
NM_001033044.4(GLUL):c.-14+892G>A	rs192236496

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