List of variants in gene IDUA reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000203.5(IDUA):c.1205G>A (p.Trp402Ter)	rs121965019	0.00086
NM_000203.5(IDUA):c.1598C>G (p.Pro533Arg)	rs121965021	0.00003
NM_000203.5(IDUA):c.1614del (p.His539fs)	rs727503967	0.00003
NM_000203.3(IDUA):c.[1225G>C;1962A>T]
NM_000203.4(IDUA):c.1960T>G (p.Ter654Gly)	rs387906504
NM_000203.5(IDUA):c.1037T>G (p.Leu346Arg)	rs121965033
NM_000203.5(IDUA):c.1091C>T (p.Thr364Met)	rs121965032
NM_000203.5(IDUA):c.1096A>C (p.Thr366Pro)	rs121965024
NM_000203.5(IDUA):c.1469T>C (p.Leu490Pro)	rs121965027
NM_000203.5(IDUA):c.1475G>C (p.Arg492Pro)	rs121965026
NM_000203.5(IDUA):c.1855C>G (p.Arg619Gly)	rs121965031
NM_000203.5(IDUA):c.1861C>T (p.Arg621Ter)	rs121965025
NM_000203.5(IDUA):c.300-3C>G	rs1226056948
NM_000203.5(IDUA):c.590-7G>A	rs762411583
NM_000203.5(IDUA):c.613_617dup (p.Glu207fs)	rs786200915
NM_000203.5(IDUA):c.898G>A (p.Ala300Thr)	rs121965030
NM_000203.5(IDUA):c.928C>T (p.Gln310Ter)	rs121965023

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