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rs7682241

From SNPedia

Orientationplus
Stabilizedplus
Make rs7682241(G;G)
Make rs7682241(G;T)
Make rs7682241(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position122602720
is asnp
is mentioned by
dbSNPrs7682241
ebirs7682241
HLIrs7682241
Exacrs7682241
Varsomers7682241
Maprs7682241
PheGenIrs7682241
hapmaprs7682241
1000 genomesrs7682241
hgdprs7682241
ensemblrs7682241
gopubmedrs7682241
geneviewrs7682241
scholarrs7682241
googlers7682241
pharmgkbrs7682241
gwascentralrs7682241
openSNPrs7682241
23andMers7682241
23andMe allrs7682241
SNP Nexus

SNPshotrs7682241
SNPdbers7682241
MSV3drs7682241
GWAS Ctlgrs7682241
GMAF0.3099
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20596022OA-icon.png]
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 17558408OA-icon.png] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.