rs767911847
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;C) | 3 | Alpha-thalassemia allele carrier |
(C;C) | 0 | common/normal |
Make rs767911847(-;-) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 177070 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs767911847 |
dbSNP (classic) | rs767911847 |
ClinGen | rs767911847 |
ebi | rs767911847 |
HLI | rs767911847 |
Exac | rs767911847 |
Gnomad | rs767911847 |
Varsome | rs767911847 |
LitVar | rs767911847 |
Map | rs767911847 |
PheGenI | rs767911847 |
Biobank | rs767911847 |
1000 genomes | rs767911847 |
hgdp | rs767911847 |
ensembl | rs767911847 |
geneview | rs767911847 |
scholar | rs767911847 |
rs767911847 | |
pharmgkb | rs767911847 |
gwascentral | rs767911847 |
openSNP | rs767911847 |
23andMe | rs767911847 |
SNPshot | rs767911847 |
SNPdbe | rs767911847 |
MSV3d | rs767911847 |
GWAS Ctlg | rs767911847 |
Max Magnitude | 3 |