Related gene-specific medical variations for Gene (Select 28231) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2615652	NM_016354.4(SLCO4A1):c.1295C>T (p.Ala432Val)	SLCO4A1, SLCO4A1-AS1 (A432V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592469	NM_016354.4(SLCO4A1):c.1450G>A (p.Val484Ile)	SLCO4A1, SLCO4A1-AS1 (V484I)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546171	NM_016354.4(SLCO4A1):c.1468G>A (p.Gly490Arg)	SLCO4A1, SLCO4A1-AS1 (G490R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2518903	NM_016354.4(SLCO4A1):c.1358C>T (p.Ala453Val)	SLCO4A1, SLCO4A1-AS1 (A453V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2479003	NM_016354.4(SLCO4A1):c.1139T>C (p.Leu380Pro)	SLCO4A1, SLCO4A1-AS1 (L380P)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2467664	NM_016354.4(SLCO4A1):c.1349G>A (p.Arg450Gln)	SLCO4A1, SLCO4A1-AS1 (R450Q)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance

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