rs7682241
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7682241(G;G) |
Make rs7682241(G;T) |
Make rs7682241(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 122602720 |
is a | snp |
is | mentioned by |
dbSNP | rs7682241 |
dbSNP (classic) | rs7682241 |
ClinGen | rs7682241 |
ebi | rs7682241 |
HLI | rs7682241 |
Exac | rs7682241 |
Gnomad | rs7682241 |
Varsome | rs7682241 |
LitVar | rs7682241 |
Map | rs7682241 |
PheGenI | rs7682241 |
Biobank | rs7682241 |
1000 genomes | rs7682241 |
hgdp | rs7682241 |
ensembl | rs7682241 |
geneview | rs7682241 |
scholar | rs7682241 |
rs7682241 | |
pharmgkb | rs7682241 |
gwascentral | rs7682241 |
openSNP | rs7682241 |
23andMe | rs7682241 |
SNPshot | rs7682241 |
SNPdbe | rs7682241 |
MSV3d | rs7682241 |
GWAS Ctlg | rs7682241 |
GMAF | 0.3099 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20596022] |
Trait | Alopecia areata |
Title | Genome-wide association study in alopecia areata implicates both innate and adaptive immunity |
Risk Allele | A |
P-val | 4E-8 |
Odds Ratio | 1.34 [1.21-1.48] |
[PMID 17558408] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.