Human SNP ID | rs12042938 |
---|---|
Human chromosome | chr1 |
Human SNP position | 231681096 |
Pig chromosome | chr14 |
Pig SNP position | 63450622 |
PubMed ID | 21483430 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/21483430 |
Study | Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. |
Disease/Trait | Neuranatomic and neurocognitive phenotypes |
Initial sample | 857 Mexican American individuals |
Replication sample | NA |
Region | 1q42.2 |
Chromosome id | chr1 |
Chromosome position | 231681096 |
Reported gene | DISC1 |
Mapped gene | DISC1, TSNAX-DISC1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 27185, 100303453 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12042938-C |
SNPs | rs12042938 |
Merged | 0 |
SNP id current | 12042938 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.48 |
P value | 4E-36 |
Pvalue mlog | 35.397940008672 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [543031] |
CNV | N |
Mapped trait | neuroimaging measurement, South Texas Assessment of Neurocognition |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004346, http://www.ebi.ac.uk/efo/EFO_0004785 |
Study accession | GCST001037 |