Human SNP ID | rs10007186 |
---|---|
Human chromosome | chr4 |
Human SNP position | 78667891 |
Pig chromosome | chr8 |
Pig SNP position | 148076787 |
PubMed ID | 22558069 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/22558069 |
Study | Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. |
Disease/Trait | Non-albumin protein levels |
Initial sample | Up to 9,103 Japanese ancestry individuals |
Replication sample | Up to 1,629 Japanese ancestry individuals |
Region | 4q21.21 |
Chromosome id | chr4 |
Chromosome position | 78667891 |
Reported gene | ANXA3 |
Mapped gene | LINC01094 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100505702 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10007186-C |
SNPs | rs10007186 |
Merged | 0 |
SNP id current | 10007186 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.307 |
P value | 0.000000001 |
Pvalue mlog | 9 |
P value text | (NAP) |
Or beta | 0.085 |
%95 Ci | [0.058-0.112] unit increase |
Platform | Illumina [2178644] (imputed) |
CNV | N |
Mapped trait | serum non-albumin protein measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004568 |
Study accession | GCST001496 |