rs424232
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs424232(A;A) |
Make rs424232(A;G) |
Make rs424232(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32240547 |
is a | snp |
is | mentioned by |
dbSNP | rs424232 |
dbSNP (classic) | rs424232 |
ClinGen | rs424232 |
ebi | rs424232 |
HLI | rs424232 |
Exac | rs424232 |
Gnomad | rs424232 |
Varsome | rs424232 |
LitVar | rs424232 |
Map | rs424232 |
PheGenI | rs424232 |
Biobank | rs424232 |
1000 genomes | rs424232 |
hgdp | rs424232 |
ensembl | rs424232 |
geneview | rs424232 |
scholar | rs424232 |
rs424232 | |
pharmgkb | rs424232 |
gwascentral | rs424232 |
openSNP | rs424232 |
23andMe | rs424232 |
SNPshot | rs424232 |
SNPdbe | rs424232 |
MSV3d | rs424232 |
GWAS Ctlg | rs424232 |
GMAF | 0.2961 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23053058] Search for schizophrenia susceptibility variants at the HLA-DRB1 locus among a British population
GWAS snp | |
---|---|
PMID | [PMID 23936387] |
Trait | Celiac disease |
Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
Risk Allele | C |
P-val | 5E-21 |
Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- 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