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rs12048904

From SNPedia

Orientationplus
Stabilizedplus
Make rs12048904(C;C)
Make rs12048904(C;T)
Make rs12048904(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position100865980
is asnp
is mentioned by
dbSNPrs12048904
dbSNP (classic)rs12048904
ClinGenrs12048904
ebirs12048904
HLIrs12048904
Exacrs12048904
Gnomadrs12048904
Varsomers12048904
LitVarrs12048904
Maprs12048904
PheGenIrs12048904
Biobankrs12048904
1000 genomesrs12048904
hgdprs12048904
ensemblrs12048904
geneviewrs12048904
scholarrs12048904
googlers12048904
pharmgkbrs12048904
gwascentralrs12048904
openSNPrs12048904
23andMers12048904
SNPshotrs12048904
SNPdbers12048904
MSV3drs12048904
GWAS Ctlgrs12048904
GMAF0.4417
Max Magnitude0
? (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 4E-8
Odds Ratio 1.0900 [1.08-1.11]