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rs2592887

From SNPedia

Orientationminus
Stabilizedminus
Make rs2592887(A;A)
Make rs2592887(A;G)
Make rs2592887(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position159683149
is asnp
is mentioned by
dbSNPrs2592887
ebirs2592887
HLIrs2592887
Exacrs2592887
Varsomers2592887
Maprs2592887
PheGenIrs2592887
hapmaprs2592887
1000 genomesrs2592887
hgdprs2592887
ensemblrs2592887
gopubmedrs2592887
geneviewrs2592887
scholarrs2592887
googlers2592887
pharmgkbrs2592887
gwascentralrs2592887
openSNPrs2592887
23andMers2592887
23andMe allrs2592887
SNP Nexus

SNPshotrs2592887
SNPdbers2592887
MSV3drs2592887
GWAS Ctlgrs2592887
GMAF0.4789
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18216863OA-icon.png] Genetic determinants of basal C-reactive protein expression in Filipino systemic lupus erythematosus families.


[PMID 18439548OA-icon.png] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.


GET Evidence
rs2592887
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.460938
summary