Human SNP ID | rs4869266 |
---|---|
Human chromosome | chr5 |
Human SNP position | 96151236 |
Pig chromosome | chr2 |
Pig SNP position | 106670636 |
PubMed ID | 23382691 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23382691 |
Study | Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. |
Disease/Trait | IgG glycosylation |
Initial sample | 2,247 European ancestry individuals |
Replication sample | NA |
Region | 5q15 |
Chromosome id | chr5 |
Chromosome position | 96151236 |
Reported gene | NR |
Mapped gene | LOC105379095, LOC101929710 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105379095, 101929710 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4869266-G |
SNPs | rs4869266 |
Merged | 0 |
SNP id current | 4869266 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.664911823953174 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (IGP16) |
Or beta | 0.1519 |
%95 Ci | [0.088-0.216] unit increase |
Platform | Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | serum IgG glycosylation measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005193 |
Study accession | GCST001848 |