Human SNP ID | rs10934011 |
---|---|
Human chromosome | chr3 |
Human SNP position | 110070723 |
Pig chromosome | chr13 |
Pig SNP position | 157776657 |
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 (parent-of-origin) |
Initial sample | 1,024 European ancestry individuals |
Replication sample | NA |
Region | 3q13.13 |
Chromosome id | chr3 |
Chromosome position | 110070723 |
Reported gene | intergenic |
Mapped gene | LOC105374035 - LOC105374036 |
Upstream gene id | 105374035 |
Downstream gene id | 105374036 |
SNP gene ids | |
Upstream gene distance | 234566 |
Downstream gene distance | 376512 |
SNP risk allele | rs10934011-G |
SNPs | rs10934011 |
Merged | 0 |
SNP id current | 10934011 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | 0.21 |
P value | 0.000000001 |
Pvalue mlog | 9 |
P value text | (NESPAS CpG08_09) |
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 | GCST002057 |