rs10181042
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10181042(C;C) |
Make rs10181042(C;T) |
Make rs10181042(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 60997124 |
Gene | PUS10 |
is a | snp |
is | mentioned by |
dbSNP | rs10181042 |
dbSNP (classic) | rs10181042 |
ClinGen | rs10181042 |
ebi | rs10181042 |
HLI | rs10181042 |
Exac | rs10181042 |
Gnomad | rs10181042 |
Varsome | rs10181042 |
LitVar | rs10181042 |
Map | rs10181042 |
PheGenI | rs10181042 |
Biobank | rs10181042 |
1000 genomes | rs10181042 |
hgdp | rs10181042 |
ensembl | rs10181042 |
geneview | rs10181042 |
scholar | rs10181042 |
rs10181042 | |
pharmgkb | rs10181042 |
gwascentral | rs10181042 |
openSNP | rs10181042 |
23andMe | rs10181042 |
SNPshot | rs10181042 |
SNPdbe | rs10181042 |
MSV3d | rs10181042 |
GWAS Ctlg | rs10181042 |
GMAF | 0.3333 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21102463] |
Trait | |
Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
Risk Allele | T |
P-val | 7E-9 |
Odds Ratio | 1.1400 [1.09-1.19] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d