Have questions? Visit https://www.reddit.com/r/SNPedia

rs6929404

From SNPedia

Orientationplus
Stabilizedplus
Make rs6929404(A;A)
Make rs6929404(A;C)
Make rs6929404(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position135132889
is asnp
is mentioned by
dbSNPrs6929404
ebirs6929404
HLIrs6929404
Exacrs6929404
Varsomers6929404
Maprs6929404
PheGenIrs6929404
hapmaprs6929404
1000 genomesrs6929404
hgdprs6929404
ensemblrs6929404
gopubmedrs6929404
geneviewrs6929404
scholarrs6929404
googlers6929404
pharmgkbrs6929404
gwascentralrs6929404
openSNPrs6929404
23andMers6929404
23andMe allrs6929404
SNP Nexus

SNPshotrs6929404
SNPdbers6929404
MSV3drs6929404
GWAS Ctlgrs6929404
GMAF0.3012
Max Magnitude
? (A;A) (A;C) (C;C) 28
OMIM142470
DescFETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2; HBFQTL2
Variant
Relatedalso
[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 18667698OA-icon.png] DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.


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