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rs9402686

From SNPedia

Orientationplus
Stabilizedplus
Make rs9402686(A;A)
Make rs9402686(A;G)
Make rs9402686(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position135106679
is asnp
is mentioned by
dbSNPrs9402686
ebirs9402686
HLIrs9402686
Exacrs9402686
Varsomers9402686
Maprs9402686
PheGenIrs9402686
hapmaprs9402686
1000 genomesrs9402686
hgdprs9402686
ensemblrs9402686
gopubmedrs9402686
geneviewrs9402686
scholarrs9402686
googlers9402686
pharmgkbrs9402686
gwascentralrs9402686
openSNPrs9402686
23andMers9402686
23andMe allrs9402686
SNP Nexus

SNPshotrs9402686
SNPdbers9402686
MSV3drs9402686
GWAS Ctlgrs9402686
GMAF0.2218
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait Hematological parameters
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele A
P-val 7E-42
Odds Ratio 0.82 [0.70-0.94] fl increase


[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 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.


GET Evidence
rs9402686
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary