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rs1845344

From SNPedia

Orientationplus
Stabilizedplus
Make rs1845344(G;G)
Make rs1845344(G;T)
Make rs1845344(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position120041230
is asnp
is mentioned by
dbSNPrs1845344
ebirs1845344
HLIrs1845344
Exacrs1845344
Varsomers1845344
Maprs1845344
PheGenIrs1845344
hapmaprs1845344
1000 genomesrs1845344
hgdprs1845344
ensemblrs1845344
gopubmedrs1845344
geneviewrs1845344
scholarrs1845344
googlers1845344
pharmgkbrs1845344
gwascentralrs1845344
openSNPrs1845344
23andMers1845344
23andMe allrs1845344
SNP Nexus

SNPshotrs1845344
SNPdbers1845344
MSV3drs1845344
GWAS Ctlgrs1845344
GMAF0.2365
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 21326311]
Trait
Title Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
Risk Allele T
P-val 0.000007
Odds Ratio 0.9700 [0.56-1.38] unit increase

[PMID 20018004OA-icon.png] A search for non-chromosome 6 susceptibility loci contributing to rheumatoid arthritis.