rs323149
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs323149(A;A) |
Make rs323149(A;T) |
Make rs323149(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 78693337 |
Gene | MAGI2 |
is a | snp |
is | mentioned by |
dbSNP | rs323149 |
dbSNP (classic) | rs323149 |
ClinGen | rs323149 |
ebi | rs323149 |
HLI | rs323149 |
Exac | rs323149 |
Gnomad | rs323149 |
Varsome | rs323149 |
LitVar | rs323149 |
Map | rs323149 |
PheGenI | rs323149 |
Biobank | rs323149 |
1000 genomes | rs323149 |
hgdp | rs323149 |
ensembl | rs323149 |
geneview | rs323149 |
scholar | rs323149 |
rs323149 | |
pharmgkb | rs323149 |
gwascentral | rs323149 |
openSNP | rs323149 |
23andMe | rs323149 |
SNPshot | rs323149 |
SNPdbe | rs323149 |
MSV3d | rs323149 |
GWAS Ctlg | rs323149 |
GMAF | 0.247 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 18720471] MAGI2 genetic variation and inflammatory bowel disease.