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rs908821

From SNPedia

Orientationminus
Stabilizedminus
Make rs908821(C;C)
Make rs908821(C;T)
Make rs908821(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position140821876
is asnp
is mentioned by
dbSNPrs908821
ebirs908821
HLIrs908821
Exacrs908821
Varsomers908821
Maprs908821
PheGenIrs908821
hapmaprs908821
1000 genomesrs908821
hgdprs908821
ensemblrs908821
gopubmedrs908821
geneviewrs908821
scholarrs908821
googlers908821
pharmgkbrs908821
gwascentralrs908821
openSNPrs908821
23andMers908821
23andMe allrs908821
SNP Nexus

SNPshotrs908821
SNPdbers908821
MSV3drs908821
GWAS Ctlgrs908821
GMAF0.3333
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000003
Odds Ratio 1.37 [NR]



[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.


GET Evidence
rs908821
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary