rs9271366

Orientation

plus

Stabilized

plus

Make rs9271366(A;A)

Make rs9271366(A;G)

Make rs9271366(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

32619077

is a	snp
is	mentioned by
dbSNP	rs9271366
dbSNP (classic)	rs9271366
ClinGen	rs9271366
ebi	rs9271366
HLI	rs9271366
Exac	rs9271366
Gnomad	rs9271366
Varsome	rs9271366
LitVar	rs9271366
Map	rs9271366
PheGenI	rs9271366
Biobank	rs9271366
1000 genomes	rs9271366
hgdp	rs9271366
ensembl	rs9271366
geneview	rs9271366
scholar	rs9271366
google	rs9271366
pharmgkb	rs9271366
gwascentral	rs9271366
openSNP	rs9271366
23andMe	rs9271366
SNPshot	rs9271366
SNPdbe	rs9271366
MSV3d	rs9271366
GWAS Ctlg	rs9271366

GMAF

0.1382

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

GWAS snp
PMID	[PMID 19525955]
Trait	Multiple sclerosis
Title	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Risk Allele	G
P-val	0
Odds Ratio	2.78 [NR]

GWAS snp
PMID	[PMID 20598377]
Trait	Multiple sclerosis
Title	Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
Risk Allele	G
P-val	4E-17
Odds Ratio	2.62 [2.09-3.28]

GWAS snp
PMID	[PMID 20694011]
Trait
Title	Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency
Risk Allele
P-val	3E-33
Odds Ratio	7.69 [5.26-11.11]

[PMID 21695597 ] MHC region and risk of systemic lupus erythematosus in African American women

GWAS snp
PMID	[PMID 21699788]
Trait
Title	HLA-Cw1202-B5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease.
Risk Allele	C
P-val	2E-70
Odds Ratio	4.4400 [3.74-5.27]

[PMID 18462017 ] Mapping the genetic architecture of gene expression in human liver.

[PMID 19143821 ] Association of MHC SNP genotype with susceptibility to type 1 diabetes: a modified survival approach.

[PMID 19838195 ] A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.

[PMID 20045101 ] Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.

[PMID 20169177 ] Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.

[PMID 20405052 ] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

[PMID 20546594 ] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.

[PMID 21408207 ] Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.

[PMID 23257407] HLA variants rs9271366 and rs9275328 are associated with systemic lupus erythematosus susceptibility in Malays and Chinese

GWAS snp
PMID	[PMID 23511034]
Trait	Ulcerative colitis
Title	Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.
Risk Allele	G
P-val	1E-18
Odds Ratio	2.10 [1.78-2.48]

[PMID 24458077 ] Association of Systemic Lupus Erythematosus Susceptibility Genes with IgA Nephropathy in a Chinese Cohort

GWAS snp
PMID	[PMID 23850713]
Trait	Crohn's disease
Title	Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Risk Allele	A
P-val	5E-12
Odds Ratio	1.66 [1.44-1.92]

[PMID 31032751] Genetic Alleles Associated with SLE Susceptibility and Clinical Manifestations in Hispanic Patients from the Dominican Republic.