Related gene-specific medical variations for Gene (Select 222553) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684452	GRCh37/hg19 6q22.2-22.31(chr6:118477336-118692304)x3	SLC35F1	Copy number gain	not provided	GUncertain significance
Select item 2672161	NM_001029858.4(SLC35F1):c.56C>G (p.Pro19Arg)	SLC35F1 (P19R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1691118	NM_001029858.4(SLC35F1):c.174-103551G>A	SLC35F1	Single nucleotide variant (intron variant)	Vascular endothelial growth factor (VEGF) inhibitor response	Gassociation
Select item 1344658	NM_001029858.4(SLC35F1):c.878T>G (p.Met293Arg)	SLC35F1 (M293R)	Single nucleotide variant (missense variant)	Nephrotic syndrome	GUncertain significance
Select item 980778	GRCh37/hg19 6q22.2-22.31(chr6:118491531-118657622)x1	SLC35F1	Copy number loss	not provided	GUncertain significance
Select item 980777	GRCh37/hg19 6q22.1-22.31(chr6:118086621-118517929)x3	SLC35F1	Copy number gain	not provided	GUncertain significance

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