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rs756699

From SNPedia

Orientationplus
Stabilizedplus
Make rs756699(C;C)
Make rs756699(C;T)
Make rs756699(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position134110884
is asnp
is mentioned by
dbSNPrs756699
ebirs756699
HLIrs756699
Exacrs756699
Varsomers756699
Maprs756699
PheGenIrs756699
hapmaprs756699
1000 genomesrs756699
hgdprs756699
ensemblrs756699
gopubmedrs756699
geneviewrs756699
scholarrs756699
googlers756699
pharmgkbrs756699
gwascentralrs756699
openSNPrs756699
23andMers756699
23andMe allrs756699
SNP Nexus

SNPshotrs756699
SNPdbers756699
MSV3drs756699
GWAS Ctlgrs756699
GMAF0.1961
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 A
P-val 6E-7
Odds Ratio 1.1200 [1.10-1.14]


[PMID 18045485OA-icon.png] The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes.