List of variants reported as likely benign for Hurler syndrome

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_000203.5(IDUA):c.1225G>C (p.Gly409Arg)	rs11934801	0.01974
NM_000203.5(IDUA):c.235G>A (p.Ala79Thr)	rs58037052	0.00910
NM_000203.5(IDUA):c.246C>G (p.His82Gln)	rs148775298	0.00274
NM_000203.5(IDUA):c.965T>A (p.Val322Glu)	rs76722191	0.00271
NM_000203.5(IDUA):c.299+1542A>T	rs387907487	0.00011
NM_000203.5(IDUA):c.299+3399C>T	rs368990025	0.00011
NM_000203.5(IDUA):c.299+1313del	rs778770773	0.00004
NM_000203.5(IDUA):c.299+1627G>A	rs387907483	0.00003
NM_000203.5(IDUA):c.299+1087G>A	rs1162410484	0.00001
NM_000203.5(IDUA):c.299+1104G>A	rs387907484	0.00001
NM_000203.5(IDUA):c.299+3322C>T	rs387907486	0.00001
NM_000203.5(IDUA):c.299+3360A>G	rs760075470	0.00001
NM_000203.5(IDUA):c.299+3410_299+3424dup	rs778682733	0.00001
NM_000203.5(IDUA):c.299+3444_299+3445del	rs758100654	0.00001
NM_000203.5(IDUA):c.299+3566G>T	rs941971930	0.00001
NM_000203.5(IDUA):c.1083G>A (p.Ala361=)	rs1553917295
NM_000203.5(IDUA):c.1161C>T (p.Leu387=)	rs1553917312
NM_000203.5(IDUA):c.299+1078del	rs1553915149
NM_000203.5(IDUA):c.299+1089del	rs1553915155
NM_000203.5(IDUA):c.299+1127del	rs1553915173
NM_000203.5(IDUA):c.299+1225G>A	rs200798328
NM_000203.5(IDUA):c.299+1235_299+1261del	rs1553915189
NM_000203.5(IDUA):c.299+1238del	rs1553915192
NM_000203.5(IDUA):c.299+1255del	rs1372086275
NM_000203.5(IDUA):c.299+1279C>T	rs387907481
NM_000203.5(IDUA):c.299+1362_299+1363del	rs1265696919
NM_000203.5(IDUA):c.299+1363dup	rs1265696919
NM_000203.5(IDUA):c.299+1414_299+1415del	rs1553915228
NM_000203.5(IDUA):c.299+1506del	rs1553915253
NM_000203.5(IDUA):c.299+1638del	rs768949918
NM_000203.5(IDUA):c.299+3410del	rs756881822
NM_000203.5(IDUA):c.299+3420del	rs1553915711
NM_000203.5(IDUA):c.299+3446A>T	rs1553915726
NM_000203.5(IDUA):c.299+3455G>T	rs752252231
NM_000203.5(IDUA):c.299+3602del	rs1553915784
NM_000203.5(IDUA):c.299+3617del	rs1553915793

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