LTC4S[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718414	NM_145867.2(LTC4S):c.24G>A (p.Leu8=)	LTC4S	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2433540	NM_145867.2(LTC4S):c.158+4A>C	LTC4S	Single nucleotide variant (intron variant)	Hypotonia-failure to thrive-microcephaly syndrome	GUncertain significance
Select item 2621818	NM_145867.2(LTC4S):c.166T>C (p.Cys56Arg)	LTC4S (C56R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3065885	NM_145867.2(LTC4S):c.229+1G>A	LTC4S	Single nucleotide variant (splice donor variant)	Asthma, nasal polyps, and aspirin intolerance	GUncertain significance
Select item 736274	NM_145867.2(LTC4S):c.229+7G>A	LTC4S	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2291067	NM_145867.2(LTC4S):c.271C>T (p.Leu91Phe)	LTC4S (L91F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238365	NM_145867.2(LTC4S):c.272T>G (p.Leu91Arg)	LTC4S (L91R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar