List of variants in gene IDUA reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000203.5(IDUA):c.352C>T (p.Leu118=)	rs3755954	0.22368
NM_000203.5(IDUA):c.543T>C (p.Asn181=)	rs6815946	0.16952
NM_000203.5(IDUA):c.1360G>A (p.Val454Ile)	rs73066479	0.16867
NM_000203.5(IDUA):c.1467C>T (p.Arg489=)	rs115929690	0.16835
NM_000203.5(IDUA):c.942G>C (p.Ala314=)	rs6830825	0.16834
NM_000203.5(IDUA):c.1081G>A (p.Ala361Thr)	rs6831280	0.16782
NM_000203.5(IDUA):c.1164G>C (p.Thr388=)	rs6836258	0.16540
NM_000203.5(IDUA):c.891C>T (p.Asn297=)	rs114806891	0.04874
NM_000203.5(IDUA):c.1174C>T (p.Leu392=)	rs201682298	0.01139
NM_000203.5(IDUA):c.346G>A (p.Gly116Arg)	rs148946496	0.00289
NM_000203.5(IDUA):c.965T>A (p.Val322Glu)	rs76722191	0.00271
NM_000203.5(IDUA):c.1403-14G>T	rs368368416	0.00016
NM_000203.5(IDUA):c.1230C>G (p.Thr410=)	rs115790973
NM_000203.5(IDUA):c.314G>A (p.Arg105Gln)	rs3755955
NM_000203.5(IDUA):c.590-8C>T	rs6848974

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