Related gene-specific medical variations for Gene (Select 10991) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 599593	NM_006841.6(SLC38A3):c.1441C>A (p.Leu481Met)	SLC38A3 (L481M)	Single nucleotide variant (missense variant)	Short stature	GUncertain significance
Select item 599592	NM_006841.6(SLC38A3):c.686T>C (p.Ile229Thr)	SLC38A3 (I229T)	Single nucleotide variant (missense variant)	Short stature	GUncertain significance
Select item 599591	NM_006841.6(SLC38A3):c.1108C>A (p.Arg370Ser)	SLC38A3 (R370S)	Single nucleotide variant (missense variant)	Short stature	GUncertain significance

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