List of variants in gene GCK reported as uncertain significance for Permanent neonatal diabetes mellitus

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.-455A>G	rs140894490	0.00101
NM_000162.5(GCK):c.-453C>T	rs191795044	0.00049
NM_000162.5(GCK):c.*11C>T	rs200698755	0.00046
NM_000162.5(GCK):c.*764C>T	rs185418856	0.00038
NM_000162.5(GCK):c.-102G>A	rs781377703	0.00023
NM_000162.5(GCK):c.213C>T (p.Val71=)	rs143128547	0.00014
NM_000162.5(GCK):c.363+9C>T	rs200985182	0.00011
NM_000162.5(GCK):c.649G>A (p.Asp217Asn)	rs147065275	0.00011
NM_000162.5(GCK):c.666C>T (p.Val222=)	rs193922318	0.00011
NM_000162.5(GCK):c.393C>T (p.Ser131=)	rs139139350	0.00009
NM_000162.5(GCK):c.363+10G>A	rs758495950	0.00006
NM_000162.5(GCK):c.*678G>T	rs555058443	0.00004
NM_000162.5(GCK):c.-279C>T	rs997877536	0.00003
NM_000162.5(GCK):c.198A>G (p.Pro66=)	rs377410513	0.00003
NM_000162.5(GCK):c.10G>A (p.Asp4Asn)	rs202091228	0.00002
NM_000162.5(GCK):c.435C>G (p.Pro145=)	rs773281783	0.00002
NM_000162.5(GCK):c.483+3G>A	rs1311596702	0.00002
NM_000162.5(GCK):c.*723A>G	rs886062345	0.00001
NM_000162.5(GCK):c.-449G>A	rs1375544246	0.00001
NM_000162.5(GCK):c.1253+12C>T	rs768491249	0.00001
NM_000162.5(GCK):c.1386G>T (p.Met462Ile)	rs193922285	0.00001
NM_000162.5(GCK):c.580-11C>T	rs370016334	0.00001
NM_000162.5(GCK):c.*270C>T	rs886062348
NM_000162.5(GCK):c.*548G>A	rs886062347
NM_000162.5(GCK):c.*721C>T	rs886062346
NM_000162.5(GCK):c.*844A>C	rs886062344
NM_000162.5(GCK):c.-102G>C	rs781377703
NM_000162.5(GCK):c.-137C>G	rs2096324530
NM_000162.5(GCK):c.-396C>G	rs2096324894
NM_000162.5(GCK):c.-456G>A	rs757266656
NM_000162.5(GCK):c.1024A>C (p.Thr342Pro)	rs1000236360
NM_000162.5(GCK):c.1120G>T (p.Val374Leu)	rs1415041911
NM_000162.5(GCK):c.1262A>G (p.Glu421Gly)	rs1257648811
NM_000162.5(GCK):c.363+10G>C	rs758495950
NM_000162.5(GCK):c.675C>T (p.Ile225=)	rs772754004
NM_000162.5(GCK):c.680-14G>C	rs577968084
NM_000162.5(GCK):c.792C>A (p.Gly264=)	rs754094813

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