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rs11968814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11968814(A;A)
Make rs11968814(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position71067268
is asnp
is mentioned by
dbSNPrs11968814
ebirs11968814
HLIrs11968814
Exacrs11968814
Varsomers11968814
Maprs11968814
PheGenIrs11968814
hapmaprs11968814
1000 genomesrs11968814
hgdprs11968814
ensemblrs11968814
gopubmedrs11968814
geneviewrs11968814
scholarrs11968814
googlers11968814
pharmgkbrs11968814
gwascentralrs11968814
openSNPrs11968814
23andMers11968814
23andMe allrs11968814
SNP Nexus

SNPshotrs11968814
SNPdbers11968814
MSV3drs11968814
GWAS Ctlgrs11968814
GMAF0.07254
Max Magnitude0
? (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 A
P-val 9E-7
Odds Ratio 1.1700 [0.70-1.64] unit decrease