Human SNP ID | rs11654699 |
---|---|
Human chromosome | chr17 |
Human SNP position | 32576292 |
Pig chromosome | chr12 |
Pig SNP position | 44159310 |
PubMed ID | 25188341 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25188341 |
Study | Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer__s Disease and Related Dementias. |
Disease/Trait | Neurofibrillary tangles |
Initial sample | up to 4,707 individuals |
Replication sample | NA |
Region | 17q11.2 |
Chromosome id | chr17 |
Chromosome position | 32576292 |
Reported gene | MYO1D |
Mapped gene | MYO1D |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4642 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11654699-C |
SNPs | rs11654699 |
Merged | 0 |
SNP id current | 11654699 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.5243 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (Ordinal II) |
Or beta | 0.2055 |
%95 Ci | [0.12-0.29] unit increase |
Platform | Affymetrix, Illumina [NR] (imputed) |
CNV | N |
Mapped trait | neurofibrilliary tangles measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006797 |
Study accession | GCST002594 |