Related gene-specific medical variations for Gene (Select 2308) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279643	NM_002015.4(FOXO1):c.275C>T (p.Ala92Val)	FOXO1, LOC130009610 (A92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643777	NM_002015.4(FOXO1):c.378G>C (p.Pro126=)	FOXO1, LOC130009609	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2480669	NM_002015.4(FOXO1):c.268G>C (p.Val90Leu)	FOXO1, LOC130009610	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384696	NM_002015.4(FOXO1):c.269T>G (p.Val90Gly)	FOXO1, LOC130009610	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227850	NM_002015.4(FOXO1):c.413C>T (p.Pro138Leu)	FOXO1, LOC130009609	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209509	NM_002015.4(FOXO1):c.281T>G (p.Val94Gly)	FOXO1, LOC130009610	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar