Related gene-specific medical variations for Gene (Select 103021296) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3319342	NM_052934.4(SLC26A9):c.103G>A (p.Glu35Lys)	SLC26A9, SLC26A9-AS1 (E35K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3319339	NM_052934.4(SLC26A9):c.15G>T (p.Arg5Ser)	SLC26A9, SLC26A9-AS1 (R5S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319338	NM_052934.4(SLC26A9):c.64G>A (p.Asp22Asn)	SLC26A9, SLC26A9-AS1 (D22N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3163903	NM_052934.4(SLC26A9):c.113G>T (p.Arg38Leu)	SLC26A9, SLC26A9-AS1 (R38L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2464334	NM_052934.4(SLC26A9):c.25G>A (p.Val9Met)	SLC26A9, SLC26A9-AS1 (V9M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380877	NM_052934.4(SLC26A9):c.20G>A (p.Arg7His)	SLC26A9, SLC26A9-AS1 (R7H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar