Human SNP ID | rs4466877 |
---|---|
Human chromosome | chr11 |
Human SNP position | 114516380 |
Pig chromosome | chr9 |
Pig SNP position | 46810940 |
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 | 11q23.2 |
Chromosome id | chr11 |
Chromosome position | 114516380 |
Reported gene | NR |
Mapped gene | LOC101926945 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101926945 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4466877-G |
SNPs | rs4466877 |
Merged | 0 |
SNP id current | 4466877 |
Context | upstream_gene_variant |
Intergenic | 0 |
Allele frequency | 0.880799535011136 |
P value | 0.0000009 |
Pvalue mlog | 6.04575749056067 |
P value text | (IGP32) |
Or beta | 0.2413 |
%95 Ci | [0.15-0.34] 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 |