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rs6659742

From SNPedia

Orientationplus
Stabilizedplus
Make rs6659742(C;C)
Make rs6659742(C;T)
Make rs6659742(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159848723
GeneC1orf204
is asnp
is mentioned by
dbSNPrs6659742
ebirs6659742
HLIrs6659742
Exacrs6659742
Varsomers6659742
Maprs6659742
PheGenIrs6659742
hapmaprs6659742
1000 genomesrs6659742
hgdprs6659742
ensemblrs6659742
gopubmedrs6659742
geneviewrs6659742
scholarrs6659742
googlers6659742
pharmgkbrs6659742
gwascentralrs6659742
openSNPrs6659742
23andMers6659742
23andMe allrs6659742
SNP Nexus

SNPshotrs6659742
SNPdbers6659742
MSV3drs6659742
GWAS Ctlgrs6659742
GMAF0.3691
Max Magnitude
? (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 7E-7
Odds Ratio 1.99 [1.52-2.61]