C1863052[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065755	NM_000603.5(NOS3):c.1951G>A (p.Gly651Arg)	NOS3 (G651R)	Single nucleotide variant (missense variant)	Alzheimer disease type 1	GUncertain significance
Select item 3632	NM_000250.2(MPO):c.2031-2A>C	MPO	Single nucleotide variant (splice acceptor variant)	Myeloperoxidase deficiency +3 more	GPathogenic/Likely pathogenic
Select item 1324732	NM_000250.2(MPO):c.249-2A>G	LOC106694315, MPO	Single nucleotide variant (splice acceptor variant)	Myeloperoxidase deficiency +1 more	GLikely pathogenic

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