Rs1186868

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Orientationplus
is asnp
is mentioned by
dbSNPrs1186868
PheGenIrs1186868
nextbiors1186868
hapmaprs1186868
1000 genomesrs1186868
hgdprs1186868
ensemblrs1186868
gopubmedrs1186868
geneviewrs1186868
scholarrs1186868
googlers1186868
pharmgkbrs1186868
gwascentralrs1186868
openSNPrs1186868
23andMers1186868
23andMe allrs1186868
SNP Nexus

SNPshotrs1186868
SNPdbers1186868
MSV3drs1186868
Chromosome2
Orientationplus
GMAF0.05556
Position61764103
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1186868(A;A)
Make rs1186868(A;G)
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.


GET Evidence
rs1186868
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary