ClinVar Miner

List of variants in gene GCK reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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NM_000162.5(GCK):c.*11C>T rs200698755
NM_000162.5(GCK):c.*297T>G rs527259972
NM_000162.5(GCK):c.*356G>A rs146107173
NM_000162.5(GCK):c.*510C>T rs141645300
NM_000162.5(GCK):c.*678G>T rs555058443
NM_000162.5(GCK):c.*735C>A rs556996030
NM_000162.5(GCK):c.*764C>T rs185418856
NM_000162.5(GCK):c.*797C>T rs2908276
NM_000162.5(GCK):c.*847G>A rs76374134
NM_000162.5(GCK):c.*92C>A rs557990162
NM_000162.5(GCK):c.208+11G>A rs77440690
NM_000162.5(GCK):c.209-8G>A rs144798843
NM_000162.5(GCK):c.333C>T (p.Pro111=) rs61736250
NM_000162.5(GCK):c.339C>T (p.Asp113=) rs149412035
NM_000162.5(GCK):c.363+10G>A rs758495950
NM_000162.5(GCK):c.393C>T (p.Ser131=) rs139139350
NM_000162.5(GCK):c.46-12C>T rs142829768
NM_000162.5(GCK):c.618G>A (p.Thr206=) rs142817246
NM_000162.5(GCK):c.645C>T (p.Tyr215=) rs144723656

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