Human SNP ID | rs2555155 |
---|---|
Human chromosome | chr11 |
Human SNP position | 6501574 |
Pig chromosome | chr9 |
Pig SNP position | 3894424 |
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 | 11p15.4 |
Chromosome id | chr11 |
Chromosome position | 6501574 |
Reported gene | FXC1, DNHD1 |
Mapped gene | DNHD1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 144132 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2555155-G |
SNPs | rs2555155 |
Merged | 0 |
SNP id current | 2555155 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.117 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (H19-ICR) |
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 |