Human SNP ID | rs3761168 |
---|---|
Human chromosome | chr20 |
Human SNP position | 8885071 |
Pig chromosome | chr17 |
Pig SNP position | 19950213 |
PubMed ID | 24564958 |
---|---|
Journal | Mol Autism |
Link | www.ncbi.nlm.nih.gov/pubmed/24564958 |
Study | Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence. |
Disease/Trait | Social communication problems |
Initial sample | Up to 5,628 European ancestry individuals |
Replication sample | NA |
Region | 20p12.3 |
Chromosome id | chr20 |
Chromosome position | 8885071 |
Reported gene | PLCB1 |
Mapped gene | PLCB1 - LOC105372522 |
Upstream gene id | 23236 |
Downstream gene id | 105372522 |
SNP gene ids | |
Upstream gene distance | 171 |
Downstream gene distance | 77128 |
SNP risk allele | rs3761168-A |
SNPs | rs3761168 |
Merged | 0 |
SNP id current | 3761168 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.05 |
P value | 0.00000008 |
Pvalue mlog | 7.09691001300805 |
P value text | (Age 17) |
Or beta | 0.32 |
%95 Ci | [0.2-0.44] unit increase |
Platform | Illumina [2293137] (imputed) |
CNV | N |
Mapped trait | social communication impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005427 |
Study accession | GCST002367 |