ClinVar Miner

List of variants in gene NAGLU reported as benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000263.4(NAGLU):c.423T>C (p.Ser141=) rs659497 0.99480
NM_000263.4(NAGLU):c.1021+120C>T rs630539 0.95964
NM_000263.4(NAGLU):c.531+50G>C rs2071046 0.74899
NM_000263.4(NAGLU):c.532-239G>C rs4792923 0.74884
NM_000263.4(NAGLU):c.532-96A>G rs2676533 0.14585
NM_000263.4(NAGLU):c.765-330T>C rs11871659 0.09948
NM_000263.4(NAGLU):c.679-78G>C rs9915710 0.07490
NM_000263.3(NAGLU):c.-138A>G rs76407245 0.06051
NM_000263.4(NAGLU):c.384-184G>C rs77469759 0.05980
NM_000263.4(NAGLU):c.1022-338C>T rs58486102 0.05975
NM_000263.4(NAGLU):c.1021+174T>C rs57188545 0.05915
NM_000263.4(NAGLU):c.1022-147G>A rs58965285 0.05906
NM_000263.4(NAGLU):c.1021+100C>T rs61661047 0.05836
NC_000017.11:g.42535761C>T rs56976372 0.04257
NM_000263.4(NAGLU):c.421T>A (p.Ser141Thr) rs61737294 0.02098
NM_000263.4(NAGLU):c.1021+274G>A rs73983733 0.02024
NM_000263.4(NAGLU):c.531+76A>G rs116738054 0.01540
NM_000263.4(NAGLU):c.675G>T (p.Leu225=) rs115680529 0.00469
NM_000263.4(NAGLU):c.679-21C>T rs77179763 0.00401
NM_000263.3(NAGLU):c.-167G>T rs145830042 0.00078
NM_000263.4(NAGLU):c.2209C>A (p.Arg737Ser) rs86312
NM_000263.4(NAGLU):c.2209C>G (p.Arg737Gly) rs86312

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