rs2160322
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2160322(C;C) |
Make rs2160322(C;G) |
Make rs2160322(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 78462650 |
Gene | MAGI2 |
is a | snp |
is | mentioned by |
dbSNP | rs2160322 |
dbSNP (classic) | rs2160322 |
ClinGen | rs2160322 |
ebi | rs2160322 |
HLI | rs2160322 |
Exac | rs2160322 |
Gnomad | rs2160322 |
Varsome | rs2160322 |
LitVar | rs2160322 |
Map | rs2160322 |
PheGenI | rs2160322 |
Biobank | rs2160322 |
1000 genomes | rs2160322 |
hgdp | rs2160322 |
ensembl | rs2160322 |
geneview | rs2160322 |
scholar | rs2160322 |
rs2160322 | |
pharmgkb | rs2160322 |
gwascentral | rs2160322 |
openSNP | rs2160322 |
23andMe | rs2160322 |
SNPshot | rs2160322 |
SNPdbe | rs2160322 |
MSV3d | rs2160322 |
GWAS Ctlg | rs2160322 |
GMAF | 0.4669 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 18720471] MAGI2 genetic variation and inflammatory bowel disease.