Have questions? Visit https://www.reddit.com/r/SNPedia

rs2116078

From SNPedia

Orientationplus
Stabilizedplus
Make rs2116078(G;G)
Make rs2116078(G;T)
Make rs2116078(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position72451754
is asnp
is mentioned by
dbSNPrs2116078
ebirs2116078
HLIrs2116078
Exacrs2116078
Varsomers2116078
Maprs2116078
PheGenIrs2116078
hapmaprs2116078
1000 genomesrs2116078
hgdprs2116078
ensemblrs2116078
gopubmedrs2116078
geneviewrs2116078
scholarrs2116078
googlers2116078
pharmgkbrs2116078
gwascentralrs2116078
openSNPrs2116078
23andMers2116078
23andMe allrs2116078
SNP Nexus

SNPshotrs2116078
SNPdbers2116078
MSV3drs2116078
GWAS Ctlgrs2116078
GMAF0.3903
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (age of onset)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000003
Odds Ratio NR NR



GET Evidence
rs2116078
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.418033
summary