Human SNP ID | rs11933531 |
---|---|
Human chromosome | chr4 |
Human SNP position | 91494378 |
Pig chromosome | chr8 |
Pig SNP position | 137047673 |
PubMed ID | 23725790 |
---|---|
Journal | Twin Res Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23725790 |
Study | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. |
Disease/Trait | DNA methylation (variation) |
Initial sample | 256 European ancestry individuals |
Replication sample | 384 European ancestry individuals |
Region | 4q22.1 |
Chromosome id | chr4 |
Chromosome position | 91494378 |
Reported gene | FAM190A |
Mapped gene | CCSER1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 401145 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11933531-A |
SNPs | rs11933531 |
Merged | 0 |
SNP id current | 11933531 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.04 |
P value | 0.00000003 |
Pvalue mlog | 7.52287874528033 |
P value text | (KvDMR) |
Or beta | |
%95 Ci | |
Platform | Illumina [515966] |
CNV | N |
Mapped trait | DNA methylation |
Mapped trait URI | http://purl.obolibrary.org/obo/GO_0006306 |
Study accession | GCST002058 |