ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_000046.3(ARSB):c.-1178A>G rs163126
NM_000046.3(ARSB):c.-840_-839dupCA rs1255033691
NM_000046.5(ARSB):c.*1257A>C rs754567
NM_000046.5(ARSB):c.*1302G>T rs754566
NM_000046.5(ARSB):c.*1469C>T rs55710452
NM_000046.5(ARSB):c.*2022T>G rs7704939
NM_000046.5(ARSB):c.*202A>G rs73770019
NM_000046.5(ARSB):c.*2654A>G
NM_000046.5(ARSB):c.*2859T>C rs116826065
NM_000046.5(ARSB):c.*2975G>T rs3088247
NM_000046.5(ARSB):c.*3181T>G rs11750774
NM_000046.5(ARSB):c.*60G>A rs2173012
NM_000046.5(ARSB):c.1072G>A (p.Val358Met) rs1065757
NM_000046.5(ARSB):c.1126G>A (p.Val376Met) rs1071598
NM_000046.5(ARSB):c.1151G>A (p.Ser384Asn) rs25414
NM_000046.5(ARSB):c.1191G>A (p.Pro397=) rs25413
NM_000046.5(ARSB):c.1362G>A (p.Pro454=) rs35757003
NM_000046.5(ARSB):c.1446A>G (p.Glu482=) rs35714924
NM_000046.5(ARSB):c.972A>G (p.Gly324=) rs72762973
NM_198709.3(ARSB):c.-302A>G rs163127

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