List of variants in gene GCK reported as likely 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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.363+317C>T	rs145391098	0.02304
NM_000162.5(GCK):c.46-5701C>T	rs73314180	0.01157
NM_000162.5(GCK):c.46-5702G>A	rs150560724	0.00865
NM_000162.5(GCK):c.679+169C>T	rs117031158	0.00775
NM_000162.5(GCK):c.864-105G>A	rs139242745	0.00743
NM_000162.5(GCK):c.46-4952G>A	rs76178320	0.00639
NM_000162.5(GCK):c.46-5594A>G	rs75119141	0.00607
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.1020-95G>A	rs540085721	0.00397
NM_000162.5(GCK):c.*92C>A	rs557990162	0.00389
NM_000162.5(GCK):c.46-4460G>T	rs539644820	0.00387
NM_000162.5(GCK):c.46-4459C>T	rs575328533	0.00384
NM_000162.5(GCK):c.1020-54G>A	rs563914015	0.00323
NM_000162.5(GCK):c.1019+18G>A	rs150914617	0.00322
NM_000162.5(GCK):c.46-62C>A	rs191196720	0.00301
NM_000162.5(GCK):c.483+14A>G	rs74852379	0.00229
NM_000162.5(GCK):c.208+11G>A	rs77440690	0.00124
NM_000162.5(GCK):c.364-18A>G	rs191255582	0.00118
NM_000162.5(GCK):c.660C>T (p.Cys220=)	rs142952813	0.00109
NM_000162.5(GCK):c.46-5598A>T	rs13306393	0.00046
NM_000162.5(GCK):c.208+17G>A	rs199822205	0.00024
NM_000162.5(GCK):c.-17C>T	rs190731555	0.00017
NM_000162.5(GCK):c.9C>T (p.Asp3=)	rs142553382	0.00009
NM_000162.5(GCK):c.863+32C>A	rs566348137	0.00007
NM_000162.5(GCK):c.600G>A (p.Val200=)	rs773561406	0.00006
NM_000162.5(GCK):c.774C>T (p.Gly258=)	rs780806456	0.00002
NM_000162.5(GCK):c.-217C>G	rs73691419
NM_000162.5(GCK):c.-267G>T	rs59914952
NM_000162.5(GCK):c.1317C>T (p.Ile439=)	rs1554334455
NM_000162.5(GCK):c.46-4438C>A	rs41282712
NM_000162.5(GCK):c.46-4438C>T	rs41282712
NM_000162.5(GCK):c.46-4988G>C	rs73314176
NM_000162.5(GCK):c.579+29G>T	rs35786405

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