List of variants in gene GALC 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000153.4(GALC):c.787G>A (p.Ala263Thr)	rs1308816724	0.00001
NM_000153.4(GALC):c.1213_1214insTA (p.Ser405fs)	rs1885266822
NM_000153.4(GALC):c.1942A>T (p.Lys648Ter)	rs1884501856
NM_000153.4(GALC):c.328+3A>G	rs377682096
NM_000153.4(GALC):c.830G>A (p.Ser277Asn)	rs1886145312

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