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rs6941421

From SNPedia

Orientationplus
Stabilizedplus
Make rs6941421(C;C)
Make rs6941421(C;T)
Make rs6941421(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position15088920
is asnp
is mentioned by
dbSNPrs6941421
ebirs6941421
HLIrs6941421
Exacrs6941421
Varsomers6941421
Maprs6941421
PheGenIrs6941421
hapmaprs6941421
1000 genomesrs6941421
hgdprs6941421
ensemblrs6941421
gopubmedrs6941421
geneviewrs6941421
scholarrs6941421
googlers6941421
pharmgkbrs6941421
gwascentralrs6941421
openSNPrs6941421
23andMers6941421
23andMe allrs6941421
SNP Nexus

SNPshotrs6941421
SNPdbers6941421
MSV3drs6941421
GWAS Ctlgrs6941421
GMAF0.3444
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 0.000006
Odds Ratio NR NR



GET Evidence
rs6941421
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary