rs3806156

Orientation

plus

Stabilized

plus

Make rs3806156(G;G)

Make rs3806156(G;T)

Make rs3806156(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

32405921

Gene	BTNL2, LOC101929163

is a	snp
is	mentioned by
dbSNP	rs3806156
dbSNP (classic)	rs3806156
ClinGen	rs3806156
ebi	rs3806156
HLI	rs3806156
Exac	rs3806156
Gnomad	rs3806156
Varsome	rs3806156
LitVar	rs3806156
Map	rs3806156
PheGenI	rs3806156
Biobank	rs3806156
1000 genomes	rs3806156
hgdp	rs3806156
ensembl	rs3806156
geneview	rs3806156
scholar	rs3806156
google	rs3806156
pharmgkb	rs3806156
gwascentral	rs3806156
openSNP	rs3806156
23andMe	rs3806156
SNPshot	rs3806156
SNPdbe	rs3806156
MSV3d	rs3806156
GWAS Ctlg	rs3806156

GMAF

0.3714

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

GWAS snp
PMID	[PMID 20410501 ]
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]

OMIM	193200
Desc
Variant
Related	also

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

[PMID 19458352 ] Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.

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

[PMID 20018063 ] 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