List of variants in gene GALC 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000153.4(GALC):c.*801A>T	rs114174103	0.01526
NM_000153.4(GALC):c.1006G>A (p.Val336Met)	rs185073540	0.00345
NM_000153.4(GALC):c.997G>A (p.Gly333Arg)	rs190921137	0.00231
NM_000153.4(GALC):c.1731C>T (p.Phe577=)	rs201560122	0.00006

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