rs7705924
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
(G;G) | 2.5 | higher odds of Crohn's disease |
Make rs7705924(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 102611094 |
Gene | LINC00491, LINC00492 |
is a | snp |
is | mentioned by |
dbSNP | rs7705924 |
dbSNP (classic) | rs7705924 |
ClinGen | rs7705924 |
ebi | rs7705924 |
HLI | rs7705924 |
Exac | rs7705924 |
Gnomad | rs7705924 |
Varsome | rs7705924 |
LitVar | rs7705924 |
Map | rs7705924 |
PheGenI | rs7705924 |
Biobank | rs7705924 |
1000 genomes | rs7705924 |
hgdp | rs7705924 |
ensembl | rs7705924 |
geneview | rs7705924 |
scholar | rs7705924 |
rs7705924 | |
pharmgkb | rs7705924 |
gwascentral | rs7705924 |
openSNP | rs7705924 |
23andMe | rs7705924 |
SNPshot | rs7705924 |
SNPdbe | rs7705924 |
MSV3d | rs7705924 |
GWAS Ctlg | rs7705924 |
GMAF | 0.06015 |
Max Magnitude | 2.5 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22412388] A genome-wide scan of ashkenazi jewish Crohn's disease suggests novel susceptibility Loci.