Human SNP ID | rs75617873 |
---|---|
Human chromosome | chr22 |
Human SNP position | 44130225 |
Pig chromosome | chr5 |
Pig SNP position | 2131888 |
PubMed ID | 23535033 |
---|---|
Journal | Alzheimers Dement |
Link | www.ncbi.nlm.nih.gov/pubmed/23535033 |
Study | Genome-wide association study of the rate of cognitive decline in Alzheimer__s disease. |
Disease/Trait | Alzheimer__s disease (cognitive decline) |
Initial sample | 303 European ancestry cases |
Replication sample | |
Region | 22q13.31 |
Chromosome id | chr22 |
Chromosome position | 44130225 |
Reported gene | PARVB |
Mapped gene | PARVB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 29780 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs75617873-? |
SNPs | rs75617873 |
Merged | 0 |
SNP id current | 75617873 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.03 |
P value | 0.0000005 |
Pvalue mlog | 6.30102999566398 |
P value text | |
Or beta | 0.17 |
%95 Ci | unit decrease |
Platform | Illumina [NR] (imputed) |
CNV | N |
Mapped trait | Alzheimers disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000249 |
Study accession | GCST001915 |