Related gene-specific medical variations for Gene (Select 9390) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3163355	NM_004256.4(SLC22A13):c.881C>T (p.Ala294Val)	LOC112935930, SLC22A13 (A294V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557649	NM_004256.4(SLC22A13):c.893A>G (p.Asn298Ser)	LOC112935930, SLC22A13 (N298S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533738	NM_004256.4(SLC22A13):c.916C>A (p.Leu306Ile)	LOC112935930, SLC22A13 (L306I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403156	NM_004256.4(SLC22A13):c.841C>T (p.Arg281Cys)	LOC112935930, SLC22A13 (R281C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348151	NM_004256.4(SLC22A13):c.925C>G (p.Gln309Glu)	LOC112935930, SLC22A13 (Q309E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240461	NM_004256.4(SLC22A13):c.823G>A (p.Ala275Thr)	LOC112935930, SLC22A13 (A275T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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