rs7776054
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7776054(A;A) |
Make rs7776054(A;G) |
Make rs7776054(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 135097778 |
is a | snp |
is | mentioned by |
dbSNP | rs7776054 |
dbSNP (classic) | rs7776054 |
ClinGen | rs7776054 |
ebi | rs7776054 |
HLI | rs7776054 |
Exac | rs7776054 |
Gnomad | rs7776054 |
Varsome | rs7776054 |
LitVar | rs7776054 |
Map | rs7776054 |
PheGenI | rs7776054 |
Biobank | rs7776054 |
1000 genomes | rs7776054 |
hgdp | rs7776054 |
ensembl | rs7776054 |
geneview | rs7776054 |
scholar | rs7776054 |
rs7776054 | |
pharmgkb | rs7776054 |
gwascentral | rs7776054 |
openSNP | rs7776054 |
23andMe | rs7776054 |
SNPshot | rs7776054 |
SNPdbe | rs7776054 |
MSV3d | rs7776054 |
GWAS Ctlg | rs7776054 |
GMAF | 0.2466 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19862010![]() |
Trait | Mean corpuscular hemoglobin |
Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
Risk Allele | G |
P-val | 7E-69 |
Odds Ratio | 0.01 [0.009-0.0111] pg decrease |
[PMID 18667698] DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
GWAS snp | |
---|---|
PMID | [PMID 23935956![]() |
Trait | Red blood cell traits |
Title | Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humans. |
Risk Allele | G |
P-val | 4E-6 |
Odds Ratio | .01 [0.0060-0.0146] unit increase |
[PMID 28361591] Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.