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

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		ClinVar version:

Total variants: 68

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HGVS	dbSNP	gnomAD frequency
NM_000202.8(IDS):c.438C>T (p.Thr146=)	rs1141608	0.32051
NM_000202.8(IDS):c.641C>T (p.Thr214Met)	rs61736892	0.01492
NM_000202.8(IDS):c.467C>A (p.Pro156Gln)	rs145231211	0.00832
NM_000202.8(IDS):c.465T>A (p.Phe155Leu)	rs149210251	0.00829
NM_000202.8(IDS):c.1269C>T (p.Pro423=)	rs61736890	0.00558
NM_000202.8(IDS):c.925A>G (p.Thr309Ala)	rs145807417	0.00488
NM_000202.8(IDS):c.754G>A (p.Asp252Asn)	rs146458524	0.00372
NM_000202.8(IDS):c.418+12T>C	rs470986	0.00178
NM_000202.8(IDS):c.825C>T (p.Asp275=)	rs148038243	0.00120
NM_000202.8(IDS):c.126C>T (p.Ile42=)	rs146963087	0.00117
NM_000202.8(IDS):c.123C>G (p.Leu41=)	rs146904022	0.00115
NM_000202.8(IDS):c.1181-13C>T	rs188486717	0.00078
NM_000202.8(IDS):c.884A>G (p.Lys295Arg)	rs113993953	0.00072
NM_000202.8(IDS):c.396G>A (p.Ser132=)	rs147108245	0.00063
NM_000202.8(IDS):c.781C>G (p.Pro261Ala)	rs141720810	0.00055
NM_000202.8(IDS):c.666C>T (p.Ala222=)	rs201588028	0.00036
NM_000202.8(IDS):c.1074C>G (p.Pro358=)	rs61736891	0.00035
NM_000202.8(IDS):c.727C>T (p.Pro243Ser)	rs143474305	0.00023
NM_000202.8(IDS):c.849G>C (p.Val283=)	rs147374356	0.00021
NM_000202.8(IDS):c.104A>G (p.Asp35Gly)	rs144081417	0.00019
NM_000202.8(IDS):c.1490A>G (p.Tyr497Cys)	rs142248439	0.00016
NM_000202.8(IDS):c.41G>A (p.Gly14Asp)	rs373389352	0.00016
NM_000202.8(IDS):c.445T>G (p.Ser149Ala)	rs146846763	0.00015
NM_000202.8(IDS):c.103+7C>T	rs369735286	0.00013
NM_000202.8(IDS):c.667G>A (p.Val223Ile)	rs200784263	0.00012
NM_000202.8(IDS):c.1499C>T (p.Thr500Ile)	rs372205468	0.00011
NM_000202.8(IDS):c.236C>G (p.Ala79Gly)	rs368513342	0.00011
NM_000202.8(IDS):c.957C>T (p.Asp319=)	rs782488487	0.00011
NM_000202.8(IDS):c.881G>A (p.Arg294Gln)	rs782445506	0.00010
NM_000202.8(IDS):c.1227G>A (p.Thr409=)	rs201905166	0.00009
NM_000202.8(IDS):c.234T>C (p.Phe78=)	rs782290556	0.00009
NM_000202.8(IDS):c.1159G>A (p.Ala387Thr)	rs376725292	0.00008
NM_000202.8(IDS):c.27C>T (p.Gly9=)	rs782412902	0.00006
NM_000202.8(IDS):c.753C>T (p.Pro251=)	rs782051908	0.00006
NM_000202.8(IDS):c.937C>T (p.Arg313Cys)	rs201048643	0.00006
NM_000202.8(IDS):c.1158C>T (p.Ser386=)	rs372340411	0.00005
NM_000202.8(IDS):c.23G>T (p.Arg8Leu)	rs782621858	0.00005
NM_000202.8(IDS):c.851C>T (p.Pro284Leu)	rs782286857	0.00005
NM_000202.8(IDS):c.868G>A (p.Val290Met)	rs782479238	0.00005
NM_000202.8(IDS):c.894G>A (p.Gln298=)	rs781812519	0.00005
NM_000202.8(IDS):c.1290G>A (p.Glu430=)	rs140633427	0.00004
NM_000202.8(IDS):c.162T>C (p.Tyr54=)	rs141088021	0.00004
NM_000202.8(IDS):c.301C>T (p.Arg101Cys)	rs782738754	0.00004
NM_000202.8(IDS):c.450G>A (p.Pro150=)	rs201892132	0.00004
NM_000202.8(IDS):c.684A>G (p.Pro228=)	rs782561677	0.00003
NM_000202.8(IDS):c.1113G>A (p.Pro371=)	rs146615651	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.696C>T (p.Phe232=)	rs782498858	0.00002
NM_000202.8(IDS):c.1143C>T (p.Leu381=)	rs781805300	0.00001
NM_000202.8(IDS):c.1181-15C>T	rs199965368	0.00001
NM_000202.8(IDS):c.13C>T (p.Arg5Trp)	rs141900718	0.00001
NM_000202.8(IDS):c.1007-7G>C	rs2124006476
NM_000202.8(IDS):c.103+5C>T	rs782108228
NM_000202.8(IDS):c.1181-14G>A
NM_000202.8(IDS):c.1327C>A (p.Arg443=)
NM_000202.8(IDS):c.1454T>C (p.Ile485Thr)
NM_000202.8(IDS):c.1548C>T (p.Asp516=)
NM_000202.8(IDS):c.418+14T>C
NM_000202.8(IDS):c.418+17A>G
NM_000202.8(IDS):c.419-16dup	rs781852261
NM_000202.8(IDS):c.419-6del	rs781852261
NM_000202.8(IDS):c.636G>A (p.Met212Ile)
NM_000202.8(IDS):c.781C>A (p.Pro261Thr)	rs141720810
NM_000202.8(IDS):c.880-11del
NM_000202.8(IDS):c.880-11dup
NM_000202.8(IDS):c.880-4G>A
NM_000202.8(IDS):c.957C>A (p.Asp319Glu)	rs782488487

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