ClinVar Miner

List of variants in gene GCK reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 24
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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.-98C>T rs200216829 0.00024
NM_000162.5(GCK):c.-102G>A rs781377703 0.00023
NM_000162.5(GCK):c.735G>A (p.Glu245=) rs775481896 0.00016
NM_000162.5(GCK):c.1288C>T (p.Leu430=) rs193922276 0.00013
NM_000162.5(GCK):c.-299A>G rs765620490 0.00012
NM_000162.5(GCK):c.-375C>T rs775776110 0.00009
NM_000162.5(GCK):c.-135G>A rs746492953 0.00003
NM_000162.3(GCK):c.-487C>G rs1329261791 0.00002
NM_000162.5(GCK):c.-452G>A rs187173652 0.00002
NM_000162.5(GCK):c.784G>A (p.Asp262Asn) rs779460424 0.00002
NM_000162.3(GCK):c.-534C>T rs182891400 0.00001
NM_000162.5(GCK):c.1319A>G (p.Glu440Gly) rs2128818815
NM_000162.5(GCK):c.207A>G (p.Ser69=) rs779548342
NM_000162.5(GCK):c.422A>C (p.His141Pro) rs2128822078
NM_000162.5(GCK):c.423C>A (p.His141Gln) rs1299283674
NM_000162.5(GCK):c.449T>A (p.Phe150Tyr) rs193922297
NM_000162.5(GCK):c.523G>A (p.Gly175Arg) rs587780344
NM_000162.5(GCK):c.632T>A (p.Ile211Asn) rs1554335400
NM_000162.5(GCK):c.749G>A (p.Arg250His) rs370375148
NM_000162.5(GCK):c.835G>A (p.Glu279Lys) rs104894005
NM_000162.5(GCK):c.835G>C (p.Glu279Gln) rs104894005
NM_000162.5(GCK):c.981C>G (p.Arg327=) rs766907428

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