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rs1318772

From SNPedia

Orientationplus
Stabilizedplus
Make rs1318772(A;A)
Make rs1318772(A;G)
Make rs1318772(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position113387870
GeneMCC
is asnp
is mentioned by
dbSNPrs1318772
ebirs1318772
HLIrs1318772
Exacrs1318772
Varsomers1318772
Maprs1318772
PheGenIrs1318772
hapmaprs1318772
1000 genomesrs1318772
hgdprs1318772
ensemblrs1318772
gopubmedrs1318772
geneviewrs1318772
scholarrs1318772
googlers1318772
pharmgkbrs1318772
gwascentralrs1318772
openSNPrs1318772
23andMers1318772
23andMe allrs1318772
SNP Nexus

SNPshotrs1318772
SNPdbers1318772
MSV3drs1318772
GWAS Ctlgrs1318772
GMAF0.1423
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 0.000001
Odds Ratio 0.9100 [0.54-1.28] unit decrease