Related gene-specific medical variations for Gene (Select 246) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690887	NM_001140.5(ALOX15):c.1180C>T (p.Arg394Ter)	ALOX15 (R394*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2647266	NM_001140.5(ALOX15):c.471A>G (p.Leu157=)	ALOX15, LOC126862468	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2556481	NM_001140.5(ALOX15):c.673G>A (p.Asp225Asn)	ALOX15, LOC126862468 (D225N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393119	NM_001140.5(ALOX15):c.589T>C (p.Trp197Arg)	ALOX15, LOC126862468 (W197R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325424	NM_001140.5(ALOX15):c.494G>A (p.Arg165Gln)	ALOX15, LOC126862468 (R165Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 730348	NM_001140.5(ALOX15):c.614G>A (p.Arg205Gln)	ALOX15, LOC126862468 (R205Q)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar