List of variants in gene GCK reported as benign by GeneDx

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.46-5883dup	rs61641319	0.99994
NM_000162.5(GCK):c.483+87A>C	rs2268573	0.57965
NM_000162.5(GCK):c.679+38T>C	rs2268574	0.57588
NM_000162.5(GCK):c.1253+8C>T	rs2908274	0.34109
NM_000162.5(GCK):c.*759del	rs55714218	0.33944
NM_000162.5(GCK):c.209-179T>C	rs12534623	0.33859
NM_000162.5(GCK):c.46-4521C>A	rs2070971	0.23160
NM_000162.5(GCK):c.209-236G>T	rs2971677	0.22722
NM_000162.5(GCK):c.1020-327C>A	rs887688	0.21332
NM_000162.5(GCK):c.46-6080G>A	rs1799831	0.21149
NM_000162.5(GCK):c.1019+174G>T	rs887686	0.18813
NM_000162.5(GCK):c.679+85A>G	rs2268575	0.17767
NM_000162.5(GCK):c.1019+257G>C	rs887687	0.17121
NC_000007.14:g.44189469C>T	rs1799884	0.17008
NM_000162.5(GCK):c.-84C>G	rs13306391	0.06548
NM_000162.5(GCK):c.*477C>T	rs2908275	0.06179
NM_000162.5(GCK):c.483+58A>T	rs115206967	0.05955
NM_000162.5(GCK):c.1253+49G>A	rs13306387	0.05898
NC_000007.14:g.44189633T>C	rs12702070	0.05341
NC_000007.14:g.44189721G>A	rs35670475	0.05248
NM_000162.5(GCK):c.484-29G>C	rs35723429	0.04382
NM_000162.5(GCK):c.46-4713G>A	rs35140467	0.02079
NM_000162.5(GCK):c.363+318G>A	rs2971678	0.01926
NM_000162.5(GCK):c.*797C>T	rs2908276	0.01885
NM_000162.5(GCK):c.46-4391T>C	rs76818786	0.01665
NM_000162.5(GCK):c.645C>T (p.Tyr215=)	rs144723656	0.00682
NM_000162.5(GCK):c.31G>A (p.Ala11Thr)	rs116093166	0.00663
NM_000162.5(GCK):c.46-12C>T	rs142829768	0.00296
NM_000162.5(GCK):c.954G>C (p.Gly318=)	rs145764627	0.00287
NM_000162.5(GCK):c.209-8G>A	rs144798843	0.00249
NM_000162.5(GCK):c.333C>T (p.Pro111=)	rs61736250	0.00235
NM_000162.5(GCK):c.1019+107T>C	rs76323047
NM_000162.5(GCK):c.1019+275del	rs5883890
NM_000162.5(GCK):c.1019+304G>C	rs2971680
NM_000162.5(GCK):c.46-5908dup	rs60650959

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