Related gene-specific medical variations for Gene (Select 11000) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 156248	NM_024330.4(SLC27A3):c.668-24C>T	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156247	NM_024330.4(SLC27A3):c.667+24C>T	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156246	NM_024330.4(SLC27A3):c.188G>T (p.Gly63Val)	SLC27A3 (G63V)	Single nucleotide variant (missense variant +1 more)	not provided	Gnot provided
Select item 156245	NM_024330.4(SLC27A3):c.1876-11C>G	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156244	NM_024330.4(SLC27A3):c.1875+15C>A	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156243	NM_024330.4(SLC27A3):c.1447+1G>A	SLC27A3	Single nucleotide variant (splice donor variant)	not provided	Gnot provided
Select item 156242	NM_024330.4(SLC27A3):c.1447+19G>A	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156241	NM_024330.4(SLC27A3):c.1161+5G>A	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 156240	NM_024330.4(SLC27A3):c.878-24C>T	SLC27A3	Single nucleotide variant (intron variant)	not provided	Gnot provided

ClinVar