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rs10017284

From SNPedia

Orientationplus
Stabilizedplus
Make rs10017284(A;A)
Make rs10017284(A;G)
Make rs10017284(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position120592060
is asnp
is mentioned by
dbSNPrs10017284
ebirs10017284
HLIrs10017284
Exacrs10017284
Varsomers10017284
Maprs10017284
PheGenIrs10017284
hapmaprs10017284
1000 genomesrs10017284
hgdprs10017284
ensemblrs10017284
gopubmedrs10017284
geneviewrs10017284
scholarrs10017284
googlers10017284
pharmgkbrs10017284
gwascentralrs10017284
openSNPrs10017284
23andMers10017284
23andMe allrs10017284
SNP Nexus

SNPshotrs10017284
SNPdbers10017284
MSV3drs10017284
GWAS Ctlgrs10017284
GMAF0.444
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000006
Odds Ratio 0.8500 [0.50-1.20] unit decrease