ClinVar Miner

List of variants in gene ARSA reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000487.6(ARSA):c.*919A>G rs5770805 0.78412
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.585G>T (p.Trp195Cys) rs6151415 0.05295
NM_000487.6(ARSA):c.*96A>G rs6151429 0.05120
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.*992G>A rs376910590 0.00717
NM_000487.6(ARSA):c.*1351C>G rs131717
NM_000487.6(ARSA):c.*777C>G rs115593886
NM_000487.6(ARSA):c.495G>A (p.Pro165=) rs145299072

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