List of variants in gene SLC35F3 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_173508.4(SLC35F3):c.829-10G>A	rs6657486	0.01811
NM_173508.4(SLC35F3):c.1338G>A (p.Glu446=)	rs34618966	0.01565
NM_173508.4(SLC35F3):c.385C>G (p.Arg129Gly)	rs34032258	0.00817

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