"SLC35C1-related condition"[Disease/phenotype] AND "PreventionGenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1904959	NM_018389.5(SLC35C1):c.336G>A (p.Arg112=)	SLC35C1	Single nucleotide variant (synonymous variant)	Leukocyte adhesion deficiency type II +1 more	GLikely benign
Select item 1534591	NM_018389.5(SLC35C1):c.630G>A (p.Ser210=)	SLC35C1	Single nucleotide variant (synonymous variant)	SLC35C1-related condition +1 more	GLikely benign
Select item 95904	NM_018389.5(SLC35C1):c.663G>A (p.Pro221=)	SLC35C1	Single nucleotide variant (synonymous variant)	SLC35C1-related condition +2 more	GConflicting classifications of pathogenicity
Select item 3053117	NM_018389.5(SLC35C1):c.717C>T (p.Cys239=)	SLC35C1	Single nucleotide variant (synonymous variant)	SLC35C1-related condition	GLikely benign
Select item 304741	NM_018389.5(SLC35C1):c.747C>T (p.Leu249=)	SLC35C1	Single nucleotide variant (synonymous variant)	SLC35C1-related condition +3 more	GConflicting classifications of pathogenicity
Select item 1161659	NM_018389.5(SLC35C1):c.858G>A (p.Leu286=)	SLC35C1	Single nucleotide variant (synonymous variant)	Leukocyte adhesion deficiency type II +1 more	GLikely benign
Select item 252721	NM_018389.5(SLC35C1):c.1054C>T (p.Pro352Ser)	SLC35C1 (P352S +1 more)	Single nucleotide variant (missense variant)	SLC35C1-related condition +3 more	GConflicting classifications of pathogenicity

ClinVar