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rs1077667

From SNPedia

Orientationminus
Stabilizedminus
Make rs1077667(A;A)
Make rs1077667(A;G)
Make rs1077667(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position6668961
GeneTNFSF14
is asnp
is mentioned by
dbSNPrs1077667
ebirs1077667
HLIrs1077667
Exacrs1077667
Varsomers1077667
Maprs1077667
PheGenIrs1077667
hapmaprs1077667
1000 genomesrs1077667
hgdprs1077667
ensemblrs1077667
gopubmedrs1077667
geneviewrs1077667
scholarrs1077667
googlers1077667
pharmgkbrs1077667
gwascentralrs1077667
openSNPrs1077667
23andMers1077667
23andMe allrs1077667
SNP Nexus

SNPshotrs1077667
SNPdbers1077667
MSV3drs1077667
GWAS Ctlgrs1077667
GMAF0.2351
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog multiple sclerosis rs1077667 TNFSF14 T 0.88
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 9E-14
Odds Ratio 1.1600 [1.14-1.18]


[PMID 23037546] Serum levels of LIGHT in MS