List of variants in gene SLC35F3 reported as likely benign for not provided

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.1461C>T (p.Ser487=)	rs754124985	0.00001
NM_173508.4(SLC35F3):c.1272T>C (p.Asn424=)
NM_173508.4(SLC35F3):c.415G>A (p.Val139Met)	rs200834507

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