List of variants in gene ARSA reported as 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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000487.6(ARSA):c.1210+20C>G	rs762674	0.76867
NM_000487.6(ARSA):c.1108-32C>T	rs762673	0.74934
NM_000487.6(ARSA):c.1178C>G (p.Thr393Ser)	rs743616	0.48362
NM_000487.5(ARSA):c.-714C>T	rs131715	0.33343
NM_000487.6(ARSA):c.1055A>G (p.Asn352Ser)	rs2071421	0.19530
NM_000487.6(ARSA):c.854+104C>T	rs6151419	0.16925
NM_000487.6(ARSA):c.854+121C>T	rs1106788	0.09187
NM_000487.6(ARSA):c.*1369C>T	rs76841085	0.07487
NM_000487.6(ARSA):c.854+156dup	rs6151420	0.06499
NM_000487.6(ARSA):c.459C>T (p.His153=)	rs6151412	0.05937
NM_000487.6(ARSA):c.1108-60C>T	rs873697	0.05763
NM_000487.6(ARSA):c.585G>T (p.Trp195Cys)	rs6151415	0.05295
NM_000487.6(ARSA):c.*96A>G	rs6151429	0.05120
NC_000022.11:g.50628271T>C	rs6151405	0.05114
NM_000487.6(ARSA):c.1493G>A (p.Arg498His)	rs6151428	0.04709
NM_000487.6(ARSA):c.684+33C>T	rs6151416	0.04666
NM_000487.6(ARSA):c.*1746G>A	rs73172277	0.04494
NM_000487.6(ARSA):c.1149C>T (p.Asp383=)	rs6151425	0.04013
NM_000487.6(ARSA):c.979+38A>G	rs6151421	0.02982
NM_000487.6(ARSA):c.*1769A>G	rs56788262	0.02807
NM_000487.6(ARSA):c.1108-77C>A	rs6151424	0.02721
NM_000487.6(ARSA):c.854+100G>A	rs6151418	0.02458
NM_000487.6(ARSA):c.243C>T (p.Gly81=)	rs6151410	0.02425
NM_000487.6(ARSA):c.624T>C (p.His208=)	rs113990230	0.01000
NM_000487.6(ARSA):c.1002C>T (p.Ser334=)	rs147027229	0.00358
NM_000487.6(ARSA):c.*1351C>G	rs131717
NM_000487.6(ARSA):c.*210A>G	rs2146714509
NM_000487.6(ARSA):c.1108-44G>A	rs950328682
NM_000487.6(ARSA):c.633G>A (p.Met211Ile)	rs773059458
NM_000487.6(ARSA):c.855-112A>G	rs762672
NM_000487.6(ARSA):c.979+13G>T	rs753874308

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