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rs17411949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs17411949(C;T)
Make rs17411949(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position140380851
GeneCLSTN2
is asnp
is mentioned by
dbSNPrs17411949
ebirs17411949
HLIrs17411949
Exacrs17411949
Varsomers17411949
Maprs17411949
PheGenIrs17411949
hapmaprs17411949
1000 genomesrs17411949
hgdprs17411949
ensemblrs17411949
gopubmedrs17411949
geneviewrs17411949
scholarrs17411949
googlers17411949
pharmgkbrs17411949
gwascentralrs17411949
openSNPrs17411949
23andMers17411949
23andMe allrs17411949
SNP Nexus

SNPshotrs17411949
SNPdbers17411949
MSV3drs17411949
GWAS Ctlgrs17411949
GMAF0.04591
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23472185OA-icon.png]
Trait Multiple sclerosis (OCB status)
Title Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Risk Allele
P-val 8E-7
Odds Ratio 1.85 [1.45-2.37]