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rs1186868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1186868(A;A)
Make rs1186868(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position61764103
GeneLOC107985767
is asnp
is mentioned by
dbSNPrs1186868
dbSNP (classic)rs1186868
ClinGenrs1186868
ebirs1186868
HLIrs1186868
Exacrs1186868
Gnomadrs1186868
Varsomers1186868
LitVarrs1186868
Maprs1186868
PheGenIrs1186868
Biobankrs1186868
1000 genomesrs1186868
hgdprs1186868
ensemblrs1186868
geneviewrs1186868
scholarrs1186868
googlers1186868
pharmgkbrs1186868
gwascentralrs1186868
openSNPrs1186868
23andMers1186868
SNPshotrs1186868
SNPdbers1186868
MSV3drs1186868
GWAS Ctlgrs1186868
GMAF0.05556
Max Magnitude0
GWAS
SNP rs1186868
PubMedID [PMID 18245381OA-icon.png]
Condition Fetal hemoglobin levels
Gene BCL11A
Risk Allele T
pValue 7.00E-035
OR 0.48
95% CI NR) SD decrease in Hb



[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.