rs731991
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs731991(A;A) |
Make rs731991(A;G) |
Make rs731991(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 30629202 |
is a | snp |
is | mentioned by |
dbSNP | rs731991 |
dbSNP (classic) | rs731991 |
ClinGen | rs731991 |
ebi | rs731991 |
HLI | rs731991 |
Exac | rs731991 |
Gnomad | rs731991 |
Varsome | rs731991 |
LitVar | rs731991 |
Map | rs731991 |
PheGenI | rs731991 |
Biobank | rs731991 |
1000 genomes | rs731991 |
hgdp | rs731991 |
ensembl | rs731991 |
geneview | rs731991 |
scholar | rs731991 |
rs731991 | |
pharmgkb | rs731991 |
gwascentral | rs731991 |
openSNP | rs731991 |
23andMe | rs731991 |
SNPshot | rs731991 |
SNPdbe | rs731991 |
MSV3d | rs731991 |
GWAS Ctlg | rs731991 |
GMAF | 0.3779 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21975197] Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk