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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000046.3(ARSB):c.-564A>G	rs59558132	0.16591
NM_000046.3(ARSB):c.-958A>G	rs57586329	0.15967
NM_000046.3(ARSB):c.-906C>G	rs62377914	0.14171
NM_000046.3(ARSB):c.*3195A>G	rs16875887	0.07068
NM_000046.5(ARSB):c.317G>A (p.Arg106His)	rs150087888	0.00230
NM_000046.5(ARSB):c.*2243A>G	rs145585943	0.00069
NM_000046.5(ARSB):c.313-12T>C	rs574816959	0.00001
NM_000046.4(ARSB):c.-322dup	rs11424557
NM_000046.4(ARSB):c.-410_-407delCTAA	rs151289643

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