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rs9389269

From SNPedia

Orientationplus
Stabilizedplus
Make rs9389269(C;C)
Make rs9389269(C;T)
Make rs9389269(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135106021
is asnp
is mentioned by
dbSNPrs9389269
ebirs9389269
HLIrs9389269
Exacrs9389269
Varsomers9389269
Maprs9389269
PheGenIrs9389269
hapmaprs9389269
1000 genomesrs9389269
hgdprs9389269
ensemblrs9389269
gopubmedrs9389269
geneviewrs9389269
scholarrs9389269
googlers9389269
pharmgkbrs9389269
gwascentralrs9389269
openSNPrs9389269
23andMers9389269
23andMe allrs9389269
SNP Nexus

SNPshotrs9389269
SNPdbers9389269
MSV3drs9389269
GWAS Ctlgrs9389269
GMAF0.2231
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele T
P-val 3E-19
Odds Ratio .60 [0.55-0.65] unit decrease


[PMID 17592125OA-icon.png] Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.


[PMID 18245381OA-icon.png] Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.


[PMID 19148297OA-icon.png] Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.


[PMID 20401335OA-icon.png] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.