ClinVar Miner

List of variants in gene SLC35D1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015139.3(SLC35D1):c.301C>T (p.Leu101Phe)	rs145382776	0.00091
NM_015139.3(SLC35D1):c.398C>T (p.Pro133Leu)	rs1558168052

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