Human SNP ID | rs8072451 |
---|---|
Human chromosome | chr17 |
Human SNP position | 45816350 |
Pig chromosome | chr12 |
Pig SNP position | 17387664 |
PubMed ID | 25607358 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/25607358 |
Study | Common genetic variants influence human subcortical brain structures. |
Disease/Trait | Subcortical brain region volumes |
Initial sample | up to 13,171 European ancestry individuals |
Replication sample | up to 15,130 European ancestry individuals, 545 Japanese ancestry individuals, 736 Mexican American individuals |
Region | 17q21.31 |
Chromosome id | chr17 |
Chromosome position | 45816350 |
Reported gene | MAPT, GRN, CRHR1, STH |
Mapped gene | MGC57346-CRHR1, CRHR1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 104909134, 1394 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs8072451-? |
SNPs | rs8072451 |
Merged | 0 |
SNP id current | 8072451 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.00000001 |
Pvalue mlog | 8 |
P value text | (Intracranial volume, EA) |
Or beta | 14489.99 |
%95 Ci | [9539.28-19440.70] unit decrease |
Platform | Affymetrix, Illumina [NR] (imputed) |
CNV | N |
Mapped trait | intra cranial volume |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004886 |
Study accession | GCST002756 |