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rs1024161

From SNPedia

Orientationplus
Stabilizedplus
Make rs1024161(C;C)
Make rs1024161(C;T)
Make rs1024161(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203857029
is asnp
is mentioned by
dbSNPrs1024161
dbSNP (classic)rs1024161
ClinGenrs1024161
ebirs1024161
HLIrs1024161
Exacrs1024161
Gnomadrs1024161
Varsomers1024161
LitVarrs1024161
Maprs1024161
PheGenIrs1024161
Biobankrs1024161
1000 genomesrs1024161
hgdprs1024161
ensemblrs1024161
geneviewrs1024161
scholarrs1024161
googlers1024161
pharmgkbrs1024161
gwascentralrs1024161
openSNPrs1024161
23andMers1024161
SNPshotrs1024161
SNPdbers1024161
MSV3drs1024161
GWAS Ctlgrs1024161
GMAF0.4982
Max Magnitude0
? (C;C) (C;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-13
Odds Ratio 1.44 [1.30-1.59]
OMIM104000
Desc
Variant
Relatedalso
GWAS snp
PMID [PMID 21841780]
Trait
Title A genome-wide association study identifies two new risk loci for Graves' disease.
Risk Allele T
P-val 2E-17
Odds Ratio 1.3000 [1.23-1.38]


[PMID 18840781OA-icon.png] Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.


[PMID 23663310OA-icon.png] Investigating highly replicated asthma genes as candidate genes for allergic rhinitis.


[PMID 30223781OA-icon.png] Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population.