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rs6952809

From SNPedia

Orientationplus
Stabilizedplus
Make rs6952809(C;C)
Make rs6952809(C;T)
Make rs6952809(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position2408858
GeneCHST12
is asnp
is mentioned by
dbSNPrs6952809
ebirs6952809
HLIrs6952809
Exacrs6952809
Varsomers6952809
Maprs6952809
PheGenIrs6952809
hapmaprs6952809
1000 genomesrs6952809
hgdprs6952809
ensemblrs6952809
gopubmedrs6952809
geneviewrs6952809
scholarrs6952809
googlers6952809
pharmgkbrs6952809
gwascentralrs6952809
openSNPrs6952809
23andMers6952809
23andMe allrs6952809
SNP Nexus

SNPshotrs6952809
SNPdbers6952809
MSV3drs6952809
GWAS Ctlgrs6952809
GMAF0.3136
Max Magnitude
? (C;C) (C;T) (T;T) 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 A
P-val 4E-6
Odds Ratio 1.08 [1.06-1.09]