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rs3806156

From SNPedia

Orientationplus
Stabilizedplus
Make rs3806156(G;G)
Make rs3806156(G;T)
Make rs3806156(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32405921
GeneBTNL2
is asnp
is mentioned by
dbSNPrs3806156
ebirs3806156
HLIrs3806156
Exacrs3806156
Varsomers3806156
Maprs3806156
PheGenIrs3806156
hapmaprs3806156
1000 genomesrs3806156
hgdprs3806156
ensemblrs3806156
gopubmedrs3806156
geneviewrs3806156
scholarrs3806156
googlers3806156
pharmgkbrs3806156
gwascentralrs3806156
openSNPrs3806156
23andMers3806156
23andMe allrs3806156
SNP Nexus

SNPshotrs3806156
SNPdbers3806156
MSV3drs3806156
GWAS Ctlgrs3806156
GMAF0.3714
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20410501OA-icon.png]
Trait Vitiligo
Title Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
Risk Allele T
P-val 7E-19
Odds Ratio 1.42 [1.32-1.54]
OMIM193200
Desc
Variant
Relatedalso


[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


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[PMID 20017995OA-icon.png] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.


[PMID 20018063OA-icon.png] Detecting significant single-nucleotide polymorphisms in a rheumatoid arthritis study using random forests.


[PMID 22991420] Genetic characterization and susceptibility for sarcoidosis in Japanese patients: risk factors of BTNL2 gene polymorphisms and HLA class II alleles