rs189984760
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs189984760(A;A) |
Make rs189984760(A;G) |
Make rs189984760(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 60511373 |
Gene | BCL11A |
is a | snp |
is | mentioned by |
dbSNP | rs189984760 |
dbSNP (classic) | rs189984760 |
ClinGen | rs189984760 |
ebi | rs189984760 |
HLI | rs189984760 |
Exac | rs189984760 |
Gnomad | rs189984760 |
Varsome | rs189984760 |
LitVar | rs189984760 |
Map | rs189984760 |
PheGenI | rs189984760 |
Biobank | rs189984760 |
1000 genomes | rs189984760 |
hgdp | rs189984760 |
ensembl | rs189984760 |
geneview | rs189984760 |
scholar | rs189984760 |
rs189984760 | |
pharmgkb | rs189984760 |
gwascentral | rs189984760 |
openSNP | rs189984760 |
23andMe | rs189984760 |
SNPshot | rs189984760 |
SNPdbe | rs189984760 |
MSV3d | rs189984760 |
GWAS Ctlg | rs189984760 |
Max Magnitude | 0 |
[PMID 28361591] Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.