"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NOS2"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 764639	NM_000625.4(NOS2):c.3333G>A (p.Glu1111=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2647576	NM_000625.4(NOS2):c.2740C>A (p.Arg914=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1335263	NM_000625.4(NOS2):c.2269C>G (p.Leu757Val)	NOS2 (L757V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2647577	NM_000625.4(NOS2):c.1755G>C (p.Leu585=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3067463	NM_000625.4(NOS2):c.1509C>T (p.Asp503=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 712632	NM_000625.4(NOS2):c.1080C>T (p.Gly360=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647578	NM_000625.4(NOS2):c.300T>C (p.Leu100=)	NOS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 624545	GRCh37/hg19 17q11.1-11.2(chr17:25403446-31685464)x3	ABHD15, ADAP2 +80 more	Copy number gain	not provided	GLikely pathogenic

ClinVar