Human SNP ID | rs3745567 |
---|---|
Human chromosome | chr19 |
Human SNP position | 6690760 |
Pig chromosome | chr2 |
Pig SNP position | 72782490 |
PubMed ID | 23028341 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23028341 |
Study | Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. |
Disease/Trait | Complement C3 and C4 levels |
Initial sample | 1,999 Han Chinese ancestry male individuals |
Replication sample | 1,496 Han Chinese ancestry male individuals |
Region | 19p13.3 |
Chromosome id | chr19 |
Chromosome position | 6690760 |
Reported gene | C3 |
Mapped gene | C3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 718 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs3745567-T |
SNPs | rs3745567 |
Merged | 0 |
SNP id current | 3745567 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.06 |
P value | 0.000000002 |
Pvalue mlog | 8.69897000433601 |
P value text | (Serum level of C3) |
Or beta | 0.09 |
%95 Ci | [0.070-0.110] g/L increase |
Platform | Illumina [1940245] (imputed) |
CNV | N |
Mapped trait | complement C3 measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004983 |
Study accession | GCST001679 |