List of variants in gene ARSA reported as benign for dementia

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_000487.6(ARSA):c.*919A>G	rs5770805	0.78412
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_000487.6(ARSA):c.*682G>C	rs7288338	0.41670
NM_000487.6(ARSA):c.*855G>A	rs7288050	0.41126
NM_000487.6(ARSA):c.*635G>A	rs5770953	0.29302
NM_000487.6(ARSA):c.*1522C>A	rs6009939	0.26325
NM_000487.6(ARSA):c.1055A>G (p.Asn352Ser)	rs2071421	0.19530
NM_000487.6(ARSA):c.*741C>T	rs8142033	0.13503
NM_000487.6(ARSA):c.*340T>A	rs5741862	0.11788
NM_000487.6(ARSA):c.*1570C>T	rs79823940	0.07507
NM_000487.6(ARSA):c.*1369C>T	rs76841085	0.07487
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
NM_000487.6(ARSA):c.1493G>A (p.Arg498His)	rs6151428	0.04709
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.*1076A>T	rs114833506	0.02807
NM_000487.6(ARSA):c.*1769A>G	rs56788262	0.02807
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.*992G>A	rs376910590	0.00717
NM_000487.6(ARSA):c.1002C>T (p.Ser334=)	rs147027229	0.00358
NM_000487.6(ARSA):c.466-7G>C	rs6151414	0.00294
NM_000487.6(ARSA):c.659C>T (p.Pro220Leu)	rs201251634	0.00261
NM_000487.6(ARSA):c.1447G>A (p.Glu483Lys)	rs148352371	0.00245
NM_000487.6(ARSA):c.982G>A (p.Val328Met)	rs143994992	0.00022
NM_000487.6(ARSA):c.636C>T (p.Ala212=)	rs200182983	0.00021
NM_000487.6(ARSA):c.972C>T (p.Ile324=)	rs200567315	0.00011
NM_000487.6(ARSA):c.1345G>A (p.Gly449Arg)	rs117341984	0.00009
NM_000487.6(ARSA):c.558C>T (p.Asn186=)	rs574416131	0.00001
NM_000487.6(ARSA):c.*1351C>G	rs131717
NM_000487.6(ARSA):c.*777C>G	rs115593886
NM_000487.6(ARSA):c.1210+13C>A	rs6151426
NM_000487.6(ARSA):c.1210+13del	rs2146717560
NM_000487.6(ARSA):c.1211-8del	rs1342017537
NM_000487.6(ARSA):c.224+12del	rs775260029
NM_000487.6(ARSA):c.495G>A (p.Pro165=)	rs145299072
NM_000487.6(ARSA):c.530G>A (p.Gly177Asp)	rs556812341
NM_000487.6(ARSA):c.598G>A (p.Glu200Lys)	rs776156197
NM_000487.6(ARSA):c.937C>A (p.Arg313=)	rs551472773

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