List of variants in gene ARSA reported as uncertain significance by Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence,

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000487.6(ARSA):c.931G>A (p.Gly311Ser)	rs74315459	0.00001
NM_000487.6(ARSA):c.1200C>T (p.Phe400=)	rs1175674325
NM_000487.6(ARSA):c.1286T>C (p.Leu429Pro)	rs1460092963
NM_000487.6(ARSA):c.190T>A (p.Phe64Ile)	rs2082698085
NM_000487.6(ARSA):c.874_883del (p.Ser292fs)	rs2082666231
NM_000487.6(ARSA):c.947C>A (p.Ala316Asp)	rs1569078754

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