rs121909829
From SNPedia
Merged into | rs33996892 |
Orientation | minus |
Stabilized | minus |
Make rs121909829(A;A) |
Make rs121909829(A;T) |
Make rs121909829(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5225608 |
Gene | HBB |
is a | snp |
is | mentioned by |
dbSNP | rs121909829 |
dbSNP (classic) | rs121909829 |
ClinGen | rs121909829 |
ebi | rs121909829 |
HLI | rs121909829 |
Exac | rs121909829 |
Gnomad | rs121909829 |
Varsome | rs121909829 |
LitVar | rs121909829 |
Map | rs121909829 |
PheGenI | rs121909829 |
Biobank | rs121909829 |
1000 genomes | rs121909829 |
hgdp | rs121909829 |
ensembl | rs121909829 |
geneview | rs121909829 |
scholar | rs121909829 |
rs121909829 | |
pharmgkb | rs121909829 |
gwascentral | rs121909829 |
openSNP | rs121909829 |
23andMe | rs121909829 |
SNPshot | rs121909829 |
SNPdbe | rs121909829 |
MSV3d | rs121909829 |
GWAS Ctlg | rs121909829 |
Status | Merged into rs33996892 |
Max Magnitude | 0 |