ClinVar Miner

List of variants in gene ARSB reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_000046.4(ARSB):c.-302A>G rs163127 0.94480
NM_000046.3(ARSB):c.-1178A>G rs163126 0.84316
NM_000046.3(ARSB):c.-1599C>T rs163125 0.81524
NM_000046.5(ARSB):c.1142+233C>T rs10039384 0.57718
NM_000046.5(ARSB):c.899-200A>G rs180049 0.39294
NM_000046.5(ARSB):c.1143-27A>C rs25415 0.35226
NM_000046.5(ARSB):c.1072G>A (p.Val358Met) rs1065757 0.34386
NM_000046.5(ARSB):c.313-26T>C rs3733895 0.30018
NM_000046.5(ARSB):c.499+160A>G rs55882246 0.26930
NM_000046.5(ARSB):c.690+271T>G rs7730261 0.26909
NM_000046.5(ARSB):c.499+145G>C rs61216659 0.26654
NM_000046.5(ARSB):c.313-81G>A rs918580 0.26591
NM_000046.5(ARSB):c.1191G>A (p.Pro397=) rs25413 0.26326
NM_000046.5(ARSB):c.313-77G>A rs918581 0.16700
NM_000046.3(ARSB):c.-564A>G rs59558132 0.16591
NM_000046.3(ARSB):c.-958A>G rs57586329 0.16084
NM_000046.5(ARSB):c.1213+23505T>C rs34152768 0.15647
NM_000046.5(ARSB):c.691-22T>C rs6870443 0.14194
NM_000046.5(ARSB):c.1142+138C>T rs79555942 0.13548
NM_000046.5(ARSB):c.691-186G>A rs11749494 0.13366
NM_000046.5(ARSB):c.1126G>A (p.Val376Met) rs1071598 0.12316
NM_000046.5(ARSB):c.500-229G>A rs10514114 0.09305
NM_000046.5(ARSB):c.1337-32C>G rs3822473 0.07773
NM_000046.5(ARSB):c.1214-32T>C rs7721866 0.07298
NM_000046.5(ARSB):c.972A>G (p.Gly324=) rs72762973 0.05293
NM_000046.5(ARSB):c.1362G>A (p.Pro454=) rs35757003 0.04998
NM_000046.5(ARSB):c.1337-217C>T rs57088170 0.04665
NM_000046.5(ARSB):c.1151G>A (p.Ser384Asn) rs25414 0.03947
NM_000046.5(ARSB):c.*202A>G rs73770019 0.03069
NM_000046.4(ARSB):c.-265G>A rs72764913 0.02482
NM_000046.5(ARSB):c.1213+22974C>T rs115179157 0.01617
NM_000046.4(ARSB):c.-322dup rs11424557
NM_000046.4(ARSB):c.-410_-407delCTAA rs151289643
NM_000046.5(ARSB):c.1213+210_1213+212del rs144799820
NM_000046.5(ARSB):c.313-286del rs34055862
NM_000046.5(ARSB):c.500-251del rs3839268
NM_000046.5(ARSB):c.500-255A>T rs338465
NM_000046.5(ARSB):c.690+136A>G rs78134348
NM_000046.5(ARSB):c.691-171_691-168del rs58376189

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