Rs1464510

Orientation

minus

is a	snp
is	mentioned by
dbSNP	rs1464510
PheGenI	rs1464510
nextbio	rs1464510
hapmap	rs1464510
1000 genomes	rs1464510
hgdp	rs1464510
ensembl	rs1464510
gopubmed	rs1464510
geneview	rs1464510
scholar	rs1464510
google	rs1464510
pharmgkb	rs1464510
gwascentral	rs1464510
openSNP	rs1464510
23andMe	rs1464510
23andMe all	rs1464510
SNP Nexus
SNPshot	rs1464510
SNPdbe	rs1464510
MSV3d	rs1464510

Gene

LPP

Chromosome

3

Orientation

minus

GMAF

0.4533

Position

188112554

Reference

GRCh37 37.1/131

Max Magnitude

Make rs1464510(G;G)

Make rs1464510(G;T)

Make rs1464510(T;T)

?	(G;G) (G;T) (T;T)	28

GWAS
SNP	rs1464510
PubMedID	[PMID 18311140]
Condition	Celiac disease
Gene	LPP
Risk Allele	A
pValue	5.00E-009
OR	1.23
95% CI	1.15-1.32

OMIM	612009
Desc	CELIAC DISEASE, SUSCEPTIBILITY TO, 11; CELIAC11
Variant
Related	also

[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort

GWAS snp
PMID	[PMID 20190752]
Trait	Celiac disease
Title	Multiple common variants for celiac disease influencing immune gene expression
Risk Allele	A
P-val	3E-40
Odds Ratio	1.29 [1.25-1.34]

GWAS snp
PMID	[PMID 20410501]
Trait	Vitiligo
Title	Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
Risk Allele	T
P-val	1E-11
Odds Ratio	1.31 [1.21-1.41]

[PMID 22087237] Improving the estimation of celiac disease sibling risk by non-HLA genes

[PMID 18853133] Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.

[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.

[PMID 20647273] Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis.

GET Evidence
rs1464510
aa_change
aa_change_short
impact	pathogenic
qualified_impact	Insufficiently evaluated pathogenic
overall_frequency	0.335938
summary