rs512770
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs512770(A;A) |
Make rs512770(A;G) |
Make rs512770(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 133258116 |
Gene | ABO |
is a | snp |
is | mentioned by |
dbSNP | rs512770 |
dbSNP (classic) | rs512770 |
ClinGen | rs512770 |
ebi | rs512770 |
HLI | rs512770 |
Exac | rs512770 |
Gnomad | rs512770 |
Varsome | rs512770 |
LitVar | rs512770 |
Map | rs512770 |
PheGenI | rs512770 |
Biobank | rs512770 |
1000 genomes | rs512770 |
hgdp | rs512770 |
ensembl | rs512770 |
geneview | rs512770 |
scholar | rs512770 |
rs512770 | |
pharmgkb | rs512770 |
gwascentral | rs512770 |
openSNP | rs512770 |
23andMe | rs512770 |
SNPshot | rs512770 |
SNPdbe | rs512770 |
MSV3d | rs512770 |
GWAS Ctlg | rs512770 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This SNP is a variant in the ABO gene, and is therefore potentially useful in determining ABO blood group, such as through the use of genosets.