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rs1841770

From SNPedia

Orientationplus
Stabilizedplus
Make rs1841770(G;G)
Make rs1841770(G;T)
Make rs1841770(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148038899
is asnp
is mentioned by
dbSNPrs1841770
ebirs1841770
HLIrs1841770
Exacrs1841770
Varsomers1841770
Maprs1841770
PheGenIrs1841770
hapmaprs1841770
1000 genomesrs1841770
hgdprs1841770
ensemblrs1841770
gopubmedrs1841770
geneviewrs1841770
scholarrs1841770
googlers1841770
pharmgkbrs1841770
gwascentralrs1841770
openSNPrs1841770
23andMers1841770
23andMe allrs1841770
SNP Nexus

SNPshotrs1841770
SNPdbers1841770
MSV3drs1841770
GWAS Ctlgrs1841770
GMAF0.2902
Max Magnitude
? (G;G) (G;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 0.000008
Odds Ratio 1.34 [NR]



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


[PMID 22411505] Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.


GET Evidence
rs1841770
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.671875
summary