Human SNP ID | rs10492972 |
---|---|
Human chromosome | chr1 |
Human SNP position | 10293054 |
Pig chromosome | chr6 |
Pig SNP position | 64513843 |
PubMed ID | 18997785 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18997785 |
Study | Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. |
Disease/Trait | Multiple sclerosis |
Initial sample | 45 European ancestry cases,195 European ancestry controls |
Replication sample | 1,316 European ancestry cases, 1,423 European ancestry controls, 1,318 cases and 1,507 controls from 756 families |
Region | 1p36.22 |
Chromosome id | chr1 |
Chromosome position | 10293054 |
Reported gene | KIF1B |
Mapped gene | KIF1B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 23095 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10492972-C |
SNPs | rs10492972 |
Merged | 0 |
SNP id current | 10492972 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.27 |
P value | 0.0000000003 |
Pvalue mlog | 9.52287874528033 |
P value text | |
Or beta | 1.34 |
%95 Ci | [1.23-1.48] |
Platform | Affymetrix [~ 250000] |
CNV | N |
Mapped trait | multiple sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003885 |
Study accession | GCST000263 |