Human SNP ID | rs7081208 |
---|---|
Human chromosome | chr10 |
Human SNP position | 13949865 |
Pig chromosome | chr10 |
Pig SNP position | 52527000 |
PubMed ID | 22430674 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/22430674 |
Study | Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer__s disease. |
Disease/Trait | Alzheimer__s disease |
Initial sample | 2,025 European ancestry cases, 5,328 European ancestry controls |
Replication sample | 7,913 European ancestry cases, 10,417 European ancestry controls |
Region | 10p13 |
Chromosome id | chr10;10;10 |
Chromosome position | 13949865;13974159;13966445 |
Reported gene | FRMD4A |
Mapped gene | FRMD4A; FRMD4A; FRMD4A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7081208-A; rs17314229-C; rs2446581-A |
SNPs | rs7081208; rs17314229; rs2446581 |
Merged | 0 |
SNP id current | |
Context | intron_variant; intron_variant; intron_variant |
Intergenic | |
Allele frequency | 0.028 |
P value | 0.0000000001 |
Pvalue mlog | 10 |
P value text | |
Or beta | 1.68 |
%95 Ci | [1.43-1.96] |
Platform | Illumina [287956] |
CNV | N |
Mapped trait | Alzheimers disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000249 |
Study accession | GCST001449 |