Human SNP ID | rs4902100 |
---|---|
Human chromosome | chr14 |
Human SNP position | 62083101 |
Pig chromosome | chr1 |
Pig SNP position | 212432501 |
PubMed ID | 24478790 |
---|---|
Journal | Front Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/24478790 |
Study | Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. |
Disease/Trait | Telomere length |
Initial sample | 4,829 European ancestry individuals from 586 families with exceptional longevity |
Replication sample | NA |
Region | 14q23.2 |
Chromosome id | chr14 |
Chromosome position | 62083101 |
Reported gene | SYT16 |
Mapped gene | SYT16 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 83851 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4902100-G |
SNPs | rs4902100 |
Merged | 0 |
SNP id current | 4902100 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.283 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | |
%95 Ci | [NR] |
Platform | Illumina [9250000] (imputed) |
CNV | N |
Mapped trait | telomere length |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004505 |
Study accession | GCST002336 |