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rs2779251

From SNPedia

Orientationplus
Stabilizedplus
Make rs2779251(A;A)
Make rs2779251(A;G)
Make rs2779251(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position27804300
is asnp
is mentioned by
dbSNPrs2779251
ebirs2779251
HLIrs2779251
Exacrs2779251
Varsomers2779251
Maprs2779251
PheGenIrs2779251
hapmaprs2779251
1000 genomesrs2779251
hgdprs2779251
ensemblrs2779251
gopubmedrs2779251
geneviewrs2779251
scholarrs2779251
googlers2779251
pharmgkbrs2779251
gwascentralrs2779251
openSNPrs2779251
23andMers2779251
23andMe allrs2779251
SNP Nexus

SNPshotrs2779251
SNPdbers2779251
MSV3drs2779251
GWAS Ctlgrs2779251
GMAF0.1244
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19074885] chronic lymphocytic leukemia rs2266690 rs17028658 rs4505265 rs1045485 rs2779251 rs3136687


[PMID 19635578] NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis


[PMID 22258388] Association of NOS2 and potential effect of VEGF, IL6, CCL2 and IL1RN polymorphisms and haplotypes on susceptibility to GCA--a simultaneous study of 130 potentially functional SNPs in 14 candidate genes

[PMID 17955236] Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility.