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rs1109670

From SNPedia

Orientationplus
Stabilizedplus
Make rs1109670(A;A)
Make rs1109670(A;C)
Make rs1109670(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position9109909
is asnp
is mentioned by
dbSNPrs1109670
ebirs1109670
HLIrs1109670
Exacrs1109670
Varsomers1109670
Maprs1109670
PheGenIrs1109670
hapmaprs1109670
1000 genomesrs1109670
hgdprs1109670
ensemblrs1109670
gopubmedrs1109670
geneviewrs1109670
scholarrs1109670
googlers1109670
pharmgkbrs1109670
gwascentralrs1109670
openSNPrs1109670
23andMers1109670
23andMe allrs1109670
SNP Nexus

SNPshotrs1109670
SNPdbers1109670
MSV3drs1109670
GWAS Ctlgrs1109670
GMAF0.2805
Max Magnitude
? (A;A) (A;C) (C;C) 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 0.000009
Odds Ratio 1.38 [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
rs1109670
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary