List of variants in gene ARSB reported as likely benign for not provided

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000046.5(ARSB):c.*60G>A	rs2173012	0.03683
NM_000046.5(ARSB):c.1213+23022G>T	rs79156343	0.03179
NM_000046.5(ARSB):c.1213+149C>G	rs73124605	0.02180
NM_000046.5(ARSB):c.1068A>T (p.Thr356=)	rs16876029	0.00947
NC_000005.10:g.78986791G>A	rs139096530	0.00836
NM_000046.5(ARSB):c.1143-263A>G	rs10044381	0.00671
NM_000046.4(ARSB):c.-246C>T	rs180784385	0.00598
NM_000046.5(ARSB):c.*1635G>A	rs35597782	0.00552
NM_000046.5(ARSB):c.*2408A>G	rs13354324	0.00491
NM_000046.5(ARSB):c.317G>A (p.Arg106His)	rs150087888	0.00230
NM_000046.5(ARSB):c.903C>T (p.Asn301=)	rs147495977	0.00106
NM_000046.5(ARSB):c.1404A>C (p.Pro468=)	rs1580961280
NM_000046.5(ARSB):c.1590C>A (p.Gly530=)	rs1580960941
NM_000046.5(ARSB):c.645C>T (p.Phe215=)

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