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rs4308217

From SNPedia

Orientationplus
Stabilizedplus
Make rs4308217(A;A)
Make rs4308217(A;C)
Make rs4308217(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position122074340
GeneCD86
is asnp
is mentioned by
dbSNPrs4308217
ebirs4308217
HLIrs4308217
Exacrs4308217
Varsomers4308217
Maprs4308217
PheGenIrs4308217
hapmaprs4308217
1000 genomesrs4308217
hgdprs4308217
ensemblrs4308217
gopubmedrs4308217
geneviewrs4308217
scholarrs4308217
googlers4308217
pharmgkbrs4308217
gwascentralrs4308217
openSNPrs4308217
23andMers4308217
23andMe allrs4308217
SNP Nexus

SNPshotrs4308217
SNPdbers4308217
MSV3drs4308217
GWAS Ctlgrs4308217
GMAF0.2397
Max Magnitude
? (A;A) (A;C) (C;C) 28
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 C
P-val 6E-8
Odds Ratio 1.10 [1.08-1.11]


[PMID 19852851OA-icon.png] Asthma and genes encoding components of the vitamin D pathway.