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rs1569723

From SNPedia

Orientationplus
Stabilizedplus
Make rs1569723(A;A)
Make rs1569723(A;C)
Make rs1569723(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position46113425
is asnp
is mentioned by
dbSNPrs1569723
ebirs1569723
HLIrs1569723
Exacrs1569723
Varsomers1569723
Maprs1569723
PheGenIrs1569723
hapmaprs1569723
1000 genomesrs1569723
hgdprs1569723
ensemblrs1569723
gopubmedrs1569723
geneviewrs1569723
scholarrs1569723
googlers1569723
pharmgkbrs1569723
gwascentralrs1569723
openSNPrs1569723
23andMers1569723
23andMe allrs1569723
SNP Nexus

SNPshotrs1569723
SNPdbers1569723
MSV3drs1569723
GWAS Ctlgrs1569723
GMAF0.2443
Max Magnitude
? (A;A) (A;C) (C;C) 28

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

OMIM126200
Desc
Variant
Relatedalso
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 20018027OA-icon.png] Conditional analysis of the major histocompatibility complex in rheumatoid arthritis.

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

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

GWAS snp
PMID [PMID 23128233OA-icon.png]
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 26474561OA-icon.png] The association of CD40 polymorphisms with CD40 serum levels and risk of systemic lupus erythematosus