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

rs10518025

From SNPedia

Orientationplus
Stabilizedplus
Make rs10518025(C;C)
Make rs10518025(C;T)
Make rs10518025(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position67198722
is asnp
is mentioned by
dbSNPrs10518025
ebirs10518025
HLIrs10518025
Exacrs10518025
Varsomers10518025
Maprs10518025
PheGenIrs10518025
hapmaprs10518025
1000 genomesrs10518025
hgdprs10518025
ensemblrs10518025
gopubmedrs10518025
geneviewrs10518025
scholarrs10518025
googlers10518025
pharmgkbrs10518025
gwascentralrs10518025
openSNPrs10518025
23andMers10518025
23andMe allrs10518025
SNP Nexus

SNPshotrs10518025
SNPdbers10518025
MSV3drs10518025
GWAS Ctlgrs10518025
GMAF0.135
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (severity)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs10518025
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary