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

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
dbSNP (classic)rs261902
ClinGenrs261902
ebirs261902
HLIrs261902
Exacrs261902
Gnomadrs261902
Varsomers261902
LitVarrs261902
Maprs261902
PheGenIrs261902
Biobankrs261902
1000 genomesrs261902
hgdprs261902
ensemblrs261902
geneviewrs261902
scholarrs261902
googlers261902
pharmgkbrs261902
gwascentralrs261902
openSNPrs261902
23andMers261902
SNPshotrs261902
SNPdbers261902
MSV3drs261902
GWAS Ctlgrs261902
GMAF0.1832
Max Magnitude0
? (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