SNP Detail For rs7672826
1.Mapping Information
Human SNP ID rs7672826
Human chromosome chr4
Human SNP position 181478542
Pig chromosome chr15
Pig SNP position 49626409
2.Annotation Information
PubMed ID19010793
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/19010793
StudyGenome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
Disease/TraitMultiple sclerosis
Initial sample978 European ancestry cases, 883 European ancestry controls
Replication sampleNA
Region4q34.3
Chromosome idchr4
Chromosome position181478542
Reported geneMGC45800
Mapped geneLOC105377574
Upstream gene id
Downstream gene id
SNP gene ids105377574
Upstream gene distance
Downstream gene distance
SNP risk allelers7672826-?
SNPsrs7672826
Merged0
SNP id current7672826
Contextintergenic_variant
Intergenic0
Allele frequency0.34
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta1.37
%95 Ci[NR]
PlatformIllumina [551642]
CNVN
Mapped traitmultiple sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003885
Study accessionGCST000269