Human SNP ID | rs1356888 |
---|---|
Human chromosome | chr2 |
Human SNP position | 50288880 |
Pig chromosome | chr3 |
Pig SNP position | 96254926 |
PubMed ID | 20834067 |
---|---|
Journal | Aging (Albany NY) |
Link | www.ncbi.nlm.nih.gov/pubmed/20834067 |
Study | Joint influence of small-effect genetic variants on human longevity. |
Disease/Trait | Longevity |
Initial sample | 1,173 individuals |
Replication sample | NA |
Region | 2p16.3 |
Chromosome id | chr2 |
Chromosome position | 50288880 |
Reported gene | NRXN1 |
Mapped gene | NRXN1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9378 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1356888-? |
SNPs | rs1356888 |
Merged | 0 |
SNP id current | 1356888 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (less than or equal to) |
Or beta | |
%95 Ci | |
Platform | NR [~ 550000] |
CNV | N |
Mapped trait | longevity |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004300 |
Study accession | GCST000785 |