rs1569723

Orientation

plus

Stabilized

plus

Make rs1569723(A;A)

Make rs1569723(A;C)

Make rs1569723(C;C)

Reference

GRCh38 38.1/141

Chromosome

20

Position

46113425

is a	snp
is	mentioned by
dbSNP	rs1569723
dbSNP (classic)	rs1569723
ClinGen	rs1569723
ebi	rs1569723
HLI	rs1569723
Exac	rs1569723
Gnomad	rs1569723
Varsome	rs1569723
LitVar	rs1569723
Map	rs1569723
PheGenI	rs1569723
Biobank	rs1569723
1000 genomes	rs1569723
hgdp	rs1569723
ensembl	rs1569723
geneview	rs1569723
scholar	rs1569723
google	rs1569723
pharmgkb	rs1569723
gwascentral	rs1569723
openSNP	rs1569723
23andMe	rs1569723
SNPshot	rs1569723
SNPdbe	rs1569723
MSV3d	rs1569723
GWAS Ctlg	rs1569723

GMAF

0.2443

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 19525955] Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

OMIM	126200
Desc
Variant
Related	also

GWAS snp
PMID	[PMID 22446961]
Trait
Title	Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.
Risk Allele	A
P-val	6E-9
Odds Ratio	1.4150 None

[PMID 20018027] Conditional analysis of the major histocompatibility complex in rheumatoid arthritis.

[PMID 20018074] Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods.

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

GWAS snp
PMID	[PMID 23128233]
Trait	Inflammatory bowel disease
Title	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele	C
P-val	1E-13
Odds Ratio	1.09 [1.056-1.126]

[PMID 26182267] [Genetic susceptibility in children with incomplete Kawasaki disease]

[PMID 26474561] The association of CD40 polymorphisms with CD40 serum levels and risk of systemic lupus erythematosus