Related gene-specific medical variations for Gene (Select 84138) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3320221	NM_032178.3(SLC7A6OS):c.835A>G (p.Arg279Gly)	SLC7A6, SLC7A6OS (R279G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3320220	NM_032178.3(SLC7A6OS):c.864C>G (p.Ser288Arg)	SLC7A6, SLC7A6OS (S288R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546449	NM_032178.3(SLC7A6OS):c.919G>T (p.Asp307Tyr)	SLC7A6, SLC7A6OS (D307Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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