SNP Detail For rs10492972
1.Mapping Information
Human SNP ID rs10492972
Human chromosome chr1
Human SNP position 10293054
Pig chromosome chr6
Pig SNP position 64513843
2.Annotation Information
PubMed ID18997785
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18997785
StudyGenetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.
Disease/TraitMultiple sclerosis
Initial sample45 European ancestry cases,195 European ancestry controls
Replication sample1,316 European ancestry cases, 1,423 European ancestry controls, 1,318 cases and 1,507 controls from 756 families
Region1p36.22
Chromosome idchr1
Chromosome position10293054
Reported geneKIF1B
Mapped geneKIF1B
Upstream gene id
Downstream gene id
SNP gene ids23095
Upstream gene distance
Downstream gene distance
SNP risk allelers10492972-C
SNPsrs10492972
Merged0
SNP id current10492972
Contextintron_variant
Intergenic0
Allele frequency0.27
P value0.0000000003
Pvalue mlog9.52287874528033
P value text
Or beta1.34
%95 Ci[1.23-1.48]
PlatformAffymetrix [~ 250000]
CNVN
Mapped traitmultiple sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003885
Study accessionGCST000263