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rs2577720

From SNPedia

Orientationminus
Stabilizedminus
Make rs2577720(G;G)
Make rs2577720(G;T)
Make rs2577720(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position23325743
is asnp
is mentioned by
dbSNPrs2577720
ebirs2577720
HLIrs2577720
Exacrs2577720
Varsomers2577720
Maprs2577720
PheGenIrs2577720
hapmaprs2577720
1000 genomesrs2577720
hgdprs2577720
ensemblrs2577720
gopubmedrs2577720
geneviewrs2577720
scholarrs2577720
googlers2577720
pharmgkbrs2577720
gwascentralrs2577720
openSNPrs2577720
23andMers2577720
23andMe allrs2577720
SNP Nexus

SNPshotrs2577720
SNPdbers2577720
MSV3drs2577720
GWAS Ctlgrs2577720
GMAF0.4509
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 C
P-val 0.000008
Odds Ratio 0.8200 [0.47-1.17] unit decrease