List of variants in gene GCK reported as likely benign for Maturity-onset diabetes of the young type 2

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.645C>T (p.Tyr215=)	rs144723656	0.00682
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.954G>C (p.Gly318=)	rs145764627	0.00287
NM_000162.5(GCK):c.*11C>T	rs200698755	0.00046
NM_000162.5(GCK):c.213C>T (p.Val71=)	rs143128547	0.00014
NM_000162.5(GCK):c.363+10G>A	rs758495950	0.00006
NM_000162.5(GCK):c.1285A>C (p.Arg429=)	rs140672134	0.00002
NM_000162.5(GCK):c.435C>G (p.Pro145=)	rs773281783	0.00002
NM_000162.5(GCK):c.1253+12C>T	rs768491249	0.00001
NM_000162.5(GCK):c.117G>A (p.Lys39=)	rs193922270
NM_000162.5(GCK):c.450C>T (p.Phe150=)	rs193922299
NM_000162.5(GCK):c.723G>A (p.Val241=)	rs193922324

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