Human SNP ID | rs7649739 |
---|---|
Human chromosome | chr3 |
Human SNP position | 65413223 |
Pig chromosome | chr13 |
Pig SNP position | 51745099 |
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 | 3p14.1 |
Chromosome id | chr3 |
Chromosome position | 65413223 |
Reported gene | NR |
Mapped gene | MAGI1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9223 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7649739-G |
SNPs | rs7649739 |
Merged | 0 |
SNP id current | 7649739 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.358836830440587 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | (IGP57) |
Or beta | 0.1501 |
%95 Ci | [0.085-0.215] unit decrease |
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 |