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rs1755289

From SNPedia

Orientationplus
Stabilizedplus
Make rs1755289(C;C)
Make rs1755289(C;T)
Make rs1755289(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position17938353
is asnp
is mentioned by
dbSNPrs1755289
ebirs1755289
HLIrs1755289
Exacrs1755289
Varsomers1755289
Maprs1755289
PheGenIrs1755289
hapmaprs1755289
1000 genomesrs1755289
hgdprs1755289
ensemblrs1755289
gopubmedrs1755289
geneviewrs1755289
scholarrs1755289
googlers1755289
pharmgkbrs1755289
gwascentralrs1755289
openSNPrs1755289
23andMers1755289
23andMe allrs1755289
SNP Nexus

SNPshotrs1755289
SNPdbers1755289
MSV3drs1755289
GWAS Ctlgrs1755289
GMAF0.4399
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000003
Odds Ratio 1.35 [NR]



[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.


GET Evidence
rs1755289
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.515625
summary