ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000046.3(ARSB):c.-840_-839dup rs1255033691 0.98775
NM_000046.4(ARSB):c.-302A>G rs163127 0.94480
NM_000046.3(ARSB):c.-1178A>G rs163126 0.84841
NM_000046.5(ARSB):c.*1302G>T rs754566 0.53627
NM_000046.5(ARSB):c.*2022T>G rs7704939 0.43898
NM_000046.5(ARSB):c.1072G>A (p.Val358Met) rs1065757 0.34419
NM_000046.5(ARSB):c.*1257A>C rs754567 0.28549
NM_000046.5(ARSB):c.1191G>A (p.Pro397=) rs25413 0.27041
NM_000046.5(ARSB):c.1126G>A (p.Val376Met) rs1071598 0.12316
NM_000046.5(ARSB):c.*3181T>G rs11750774 0.09828
NM_000046.5(ARSB):c.*1469C>T rs55710452 0.06599
NM_000046.5(ARSB):c.972A>G (p.Gly324=) rs72762973 0.05483
NM_000046.5(ARSB):c.1362G>A (p.Pro454=) rs35757003 0.04998
NM_000046.5(ARSB):c.1151G>A (p.Ser384Asn) rs25414 0.03947
NM_000046.5(ARSB):c.*60G>A rs2173012 0.03683
NM_000046.5(ARSB):c.*202A>G rs73770019 0.03289
NM_000046.5(ARSB):c.1446A>G (p.Glu482=) rs35714924 0.01223
NM_000046.5(ARSB):c.*2859T>C rs116826065 0.00988
NM_000046.5(ARSB):c.*2654A>G rs147170505 0.00961
NM_000046.5(ARSB):c.*2975G>T rs3088247

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