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rs261902

From SNPedia

Orientationminus
Stabilizedminus
Make rs261902(C;C)
Make rs261902(C;T)
Make rs261902(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position32323793
GeneBICD1
is asnp
is mentioned by
dbSNPrs261902
ebirs261902
HLIrs261902
Exacrs261902
Varsomers261902
Maprs261902
PheGenIrs261902
hapmaprs261902
1000 genomesrs261902
hgdprs261902
ensemblrs261902
gopubmedrs261902
geneviewrs261902
scholarrs261902
googlers261902
pharmgkbrs261902
gwascentralrs261902
openSNPrs261902
23andMers261902
23andMe allrs261902
SNP Nexus

SNPshotrs261902
SNPdbers261902
MSV3drs261902
GWAS Ctlgrs261902
GMAF0.1832
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Normalized brain volume
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
rs261902
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.804688
summary