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rs12368653

From SNPedia

Orientationplus
Stabilizedplus
Make rs12368653(A;A)
Make rs12368653(A;G)
Make rs12368653(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position57739473
GeneAGAP2
is asnp
is mentioned by
dbSNPrs12368653
ebirs12368653
HLIrs12368653
Exacrs12368653
Varsomers12368653
Maprs12368653
PheGenIrs12368653
hapmaprs12368653
1000 genomesrs12368653
hgdprs12368653
ensemblrs12368653
gopubmedrs12368653
geneviewrs12368653
scholarrs12368653
googlers12368653
pharmgkbrs12368653
gwascentralrs12368653
openSNPrs12368653
23andMers12368653
23andMe allrs12368653
SNP Nexus

SNPshotrs12368653
SNPdbers12368653
MSV3drs12368653
GWAS Ctlgrs12368653
GMAF0.3168
Max Magnitude
? (A;A) (A;G) (G;G) 28

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

OMIM126200
Desc
Variant
Relatedalso
[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 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 2E-9
Odds Ratio 1.10 [1.09-1.12]