Basic information of COX2 :

Official Symbol of Gene	COX2
Species	Homo sapiens neanderthalensis (common: Neandertal, sub-species: neanderthalensis)
Entrez Gene ID	6775079
Official Full Name	N/A
Also known as	N/A
Gene Type	protein coding
dbXrefs	N/A
Map Location	Chromosome: MT; NC_011137.1 (7581..8264)
Variation Type	polymorphisms in this COX-2 region
refSNP ID	765G>C and 62C>G

Sample information of multiple sclerosis:

Detected Sample	peripheral blood
Sample Detail	Genomic DNA
Detected Method	RG-PCR
Disease	MS
Disease subtype	RRMS、PPMS、SPMS
Population	Italy
Sample Size	159 patients with MS,215 healthy donors

Literature information of multiple sclerosis :

Pubmed ID	17373929
Year	2007
Title	ckwell Publishing Ltd COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of 765G>C with disease risk

Results of multiple sclerosis :

Risk Type	N/A
Main Result	Negative
Result	polymorphisms in this COX-2 region are unlikely to be involved in MS susceptibility.
Mechanism/Pathway	N/A