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rs7748513

From SNPedia

Orientationplus
Stabilizedplus
Make rs7748513(A;A)
Make rs7748513(A;G)
Make rs7748513(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position41160234
GeneTREM2
is asnp
is mentioned by
dbSNPrs7748513
ebirs7748513
HLIrs7748513
Exacrs7748513
Varsomers7748513
Maprs7748513
PheGenIrs7748513
hapmaprs7748513
1000 genomesrs7748513
hgdprs7748513
ensemblrs7748513
gopubmedrs7748513
geneviewrs7748513
scholarrs7748513
googlers7748513
pharmgkbrs7748513
gwascentralrs7748513
openSNPrs7748513
23andMers7748513
23andMe allrs7748513
SNP Nexus

SNPshotrs7748513
SNPdbers7748513
MSV3drs7748513
GWAS Ctlgrs7748513
GMAF0.1354
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22939635OA-icon.png]
Trait C-reactive protein
Title Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
Risk Allele G
P-val 1E-10
Odds Ratio NR NR


[PMID 19019460OA-icon.png] No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.