Human SNP ID | rs965808 |
---|---|
Human chromosome | chr20 |
Human SNP position | 58833371 |
Pig chromosome | chr17 |
Pig SNP position | 66298079 |
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 | 20q13.32 |
Chromosome id | chr20 |
Chromosome position | 58833371 |
Reported gene | GNAS, GNAS-AS1 |
Mapped gene | GNAS-AS1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 149775 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs965808-G |
SNPs | rs965808 |
Merged | 0 |
SNP id current | 965808 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.22 |
P value | 0.000000005 |
Pvalue mlog | 8.30102999566398 |
P value text | (NESPAS-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 |