rs1495465
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1495465(G;T) |
Make rs1495465(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 57549696 |
Gene | LOC105370519 |
is a | snp |
is | mentioned by |
dbSNP | rs1495465 |
dbSNP (classic) | rs1495465 |
ClinGen | rs1495465 |
ebi | rs1495465 |
HLI | rs1495465 |
Exac | rs1495465 |
Gnomad | rs1495465 |
Varsome | rs1495465 |
LitVar | rs1495465 |
Map | rs1495465 |
PheGenI | rs1495465 |
Biobank | rs1495465 |
1000 genomes | rs1495465 |
hgdp | rs1495465 |
ensembl | rs1495465 |
geneview | rs1495465 |
scholar | rs1495465 |
rs1495465 | |
pharmgkb | rs1495465 |
gwascentral | rs1495465 |
openSNP | rs1495465 |
23andMe | rs1495465 |
SNPshot | rs1495465 |
SNPdbe | rs1495465 |
MSV3d | rs1495465 |
GWAS Ctlg | rs1495465 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19334001] Contribution of IL23R but not ATG16L1 to Crohn's disease susceptibility in Koreans