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rs13279485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs13279485(C;C)
Make rs13279485(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position1935186
GeneARHGEF10, PRPH2
is asnp
is mentioned by
dbSNPrs13279485
ebirs13279485
HLIrs13279485
Exacrs13279485
Varsomers13279485
Maprs13279485
PheGenIrs13279485
hapmaprs13279485
1000 genomesrs13279485
hgdprs13279485
ensemblrs13279485
gopubmedrs13279485
geneviewrs13279485
scholarrs13279485
googlers13279485
pharmgkbrs13279485
gwascentralrs13279485
openSNPrs13279485
23andMers13279485
23andMe allrs13279485
SNP Nexus

SNPshotrs13279485
SNPdbers13279485
MSV3drs13279485
GWAS Ctlgrs13279485
GMAF0.03994
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 1E-6
Odds Ratio NR NR