Related gene-specific medical variations for Gene (Select 9450) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531192	NM_004271.4(LY86):c.109G>A (p.Gly37Ser)	LY86, LY86-AS1 (G37S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306068	NM_004271.4(LY86):c.7G>T (p.Gly3Cys)	LY86, LY86-AS1 (G3C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 782469	NM_004271.4(LY86):c.30C>T (p.Leu10=)	LY86, LY86-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign

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