List of variants in gene GCK reported as benign for not specified

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.1253+8C>T	rs2908274	0.34109
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.339C>T (p.Asp113=)	rs149412035	0.00451
NM_000162.5(GCK):c.618G>A (p.Thr206=)	rs142817246	0.00400
NM_000162.5(GCK):c.1019+18G>A	rs150914617	0.00322
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.483+14A>G	rs74852379	0.00229
NM_000162.5(GCK):c.660C>T (p.Cys220=)	rs142952813	0.00109
NM_000162.5(GCK):c.-215A>G	rs13306390	0.00065
NM_000162.5(GCK):c.*11C>T	rs200698755	0.00046
NM_000162.5(GCK):c.364-13G>A	rs372405219	0.00015
NM_000162.5(GCK):c.666C>T (p.Val222=)	rs193922318	0.00011
NM_000162.5(GCK):c.9C>T (p.Asp3=)	rs142553382	0.00009
NM_000162.5(GCK):c.363+10G>A	rs758495950	0.00006
NM_000162.5(GCK):c.138G>A (p.Arg46=)	rs550111033	0.00003

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