ClinVar Miner

List of variants in gene GAN reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_022041.4(GAN):c.670T>G (p.Ser224Ala) rs139055455 0.00022
NM_022041.4(GAN):c.1630G>A (p.Val544Met) rs200071978 0.00010
NM_022041.4(GAN):c.490G>A (p.Val164Ile) rs778744880 0.00003
NM_022041.4(GAN):c.972A>T (p.Ala324=) rs1430569033 0.00003
NM_022041.4(GAN):c.1132A>G (p.Ile378Val) rs571347913 0.00002
NM_022041.4(GAN):c.1171A>G (p.Met391Val) rs367600164 0.00002
NM_022041.4(GAN):c.1678C>T (p.Leu560Phe) rs143179676 0.00002
NM_022041.4(GAN):c.1241G>A (p.Gly414Asp) rs761827117 0.00001
NM_022041.4(GAN):c.1391G>A (p.Cys464Tyr) rs777535272 0.00001
NM_022041.4(GAN):c.1628A>G (p.Tyr543Cys) rs879253958 0.00001
NM_022041.4(GAN):c.236C>T (p.Ser79Leu) rs1310137430 0.00001
NM_022041.4(GAN):c.1139G>T (p.Gly380Val) rs1427637335
NM_022041.4(GAN):c.1259A>C (p.Lys420Thr) rs879254174
NM_022041.4(GAN):c.1315G>A (p.Glu439Lys) rs2150691652
NM_022041.4(GAN):c.1327C>G (p.Pro443Ala) rs150043237
NM_022041.4(GAN):c.1381G>A (p.Ala461Thr) rs766155831
NM_022041.4(GAN):c.421G>T (p.Ala141Ser) rs1057524254
NM_022041.4(GAN):c.500C>G (p.Thr167Arg)
NM_022041.4(GAN):c.565G>T (p.Val189Phe) rs766484755
NM_022041.4(GAN):c.679G>T (p.Asp227Tyr) rs1265208461
NM_022041.4(GAN):c.776G>C (p.Gly259Ala)

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