ClinVar Miner

List of variants in gene ARSB reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
GRCh37/hg19 5q14.1(chr5:78106062-78111731)x1
GRCh37/hg19 5q14.1(chr5:78106062-78115511)x1
GRCh37/hg19 5q14.1(chr5:78110117-78111731)x1
GRCh37/hg19 5q14.1(chr5:78110117-78115511)x1
GRCh37/hg19 5q14.1(chr5:78110117-78150147)x1
GRCh37/hg19 5q14.1(chr5:78110117-78180736)x1
GRCh37/hg19 5q14.1(chr5:78153325-78246593)x3
GRCh37/hg19 5q14.1(chr5:78153325-78250133)x3
GRCh37/hg19 5q14.1(chr5:78280531-78280745)x4
GRCh37/hg19 5q14.1(chr5:78280531-78281153)x1
GRCh37/hg19 5q14.1(chr5:78280531-78281245)x4
GRCh37/hg19 5q14.1(chr5:78280531-78287810)x0
GRCh37/hg19 5q14.1(chr5:78280531-78292577)x1
NM_000046.3(ARSB):c.1126G>A (p.Val376Met) rs1071598
NM_000046.3(ARSB):c.1191G>A (p.Pro397=) rs25413
NM_000046.3(ARSB):c.1362G>A (p.Pro454=) rs35757003
NM_000046.3(ARSB):c.313-26T>C rs3733895
NM_000046.3(ARSB):c.972A>G (p.Gly324=) rs72762973
NM_000046.4(ARSB):c.1143-27A>C rs25415
NM_000046.4(ARSB):c.1151G>A (p.Ser384Asn) rs25414
NM_000046.4(ARSB):c.691-22T>C rs6870443

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