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rs386965

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Orientationminus
Stabilizedminus
Make rs386965(A;A)
Make rs386965(A;G)
Make rs386965(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position79618644
is asnp
is mentioned by
dbSNPrs386965
ebirs386965
HLIrs386965
Exacrs386965
Varsomers386965
Maprs386965
PheGenIrs386965
hapmaprs386965
1000 genomesrs386965
hgdprs386965
ensemblrs386965
gopubmedrs386965
geneviewrs386965
scholarrs386965
googlers386965
pharmgkbrs386965
gwascentralrs386965
openSNPrs386965
23andMers386965
23andMe allrs386965
SNP Nexus

SNPshotrs386965
SNPdbers386965
MSV3drs386965
GWAS Ctlgrs386965
GMAF0.3737
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 4E-6
Odds Ratio 1.09 [1.07-1.11]