List of variants in gene IDS reported as benign for Mucopolysaccharidosis, MPS-II

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000202.8(IDS):c.418+12T>C	rs470986	0.00736
NM_000202.8(IDS):c.1269C>T (p.Pro423=)	rs61736890	0.00513
NM_000202.8(IDS):c.123C>G (p.Leu41=)	rs146904022	0.00115
NM_000202.8(IDS):c.126C>T (p.Ile42=)	rs146963087	0.00115
NM_000202.8(IDS):c.1181-13C>T	rs188486717	0.00081
NM_000202.8(IDS):c.396G>A (p.Ser132=)	rs147108245	0.00063
NM_000202.8(IDS):c.104A>G (p.Asp35Gly)	rs144081417	0.00020
NM_000202.8(IDS):c.1490A>G (p.Tyr497Cys)	rs142248439	0.00015
NM_000202.8(IDS):c.103+7C>T	rs369735286	0.00011
NM_000202.8(IDS):c.236C>G (p.Ala79Gly)	rs368513342	0.00011
NM_000202.8(IDS):c.1499C>T (p.Thr500Ile)	rs372205468	0.00010
NM_000202.8(IDS):c.1227G>A (p.Thr409=)	rs201905166	0.00009
NM_000202.8(IDS):c.162T>C (p.Tyr54=)	rs141088021	0.00007
NM_000202.8(IDS):c.234T>C (p.Phe78=)	rs782290556	0.00006
NM_000202.8(IDS):c.1290G>A (p.Glu430=)	rs140633427	0.00004
NM_000202.8(IDS):c.301C>T (p.Arg101Cys)	rs782738754	0.00004
NM_000202.8(IDS):c.1181-14G>A	rs200950988	0.00002
NM_000202.8(IDS):c.1181-15C>T	rs199965368	0.00002
NM_000202.8(IDS):c.1347G>A (p.Glu449=)	rs782690963	0.00002
NM_000202.8(IDS):c.177G>A (p.Val59=)	rs782743276	0.00002
NM_000202.8(IDS):c.1327C>A (p.Arg443=)	rs199422227	0.00001
NM_000202.8(IDS):c.418+14T>C	rs781915630	0.00001
NM_000202.8(IDS):c.103+5C>T	rs782108228
NM_000202.8(IDS):c.1454T>C (p.Ile485Thr)	rs782430567
NM_000202.8(IDS):c.1548C>T (p.Asp516=)	rs782433387
NM_000202.8(IDS):c.418+17A>G	rs1210262255

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