rs4150167
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs4150167(A;A) |
| Make rs4150167(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 84180078 |
| Gene | TAF1C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4150167 |
| dbSNP (classic) | rs4150167 |
| ClinGen | rs4150167 |
| ebi | rs4150167 |
| HLI | rs4150167 |
| Exac | rs4150167 |
| Gnomad | rs4150167 |
| Varsome | rs4150167 |
| LitVar | rs4150167 |
| Map | rs4150167 |
| PheGenI | rs4150167 |
| Biobank | rs4150167 |
| 1000 genomes | rs4150167 |
| hgdp | rs4150167 |
| ensembl | rs4150167 |
| geneview | rs4150167 |
| scholar | rs4150167 |
| rs4150167 | |
| pharmgkb | rs4150167 |
| gwascentral | rs4150167 |
| openSNP | rs4150167 |
| 23andMe | rs4150167 |
| SNPshot | rs4150167 |
| SNPdbe | rs4150167 |
| MSV3d | rs4150167 |
| GWAS Ctlg | rs4150167 |
| GMAF | 0.008724 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22843504 ]
|
| Trait | Autism |
| Title | Individual common variants exert weak effects on the risk for autism spectrum disorderspi. |
| Risk Allele | |
| P-val | 3E-7 |
| Odds Ratio | 1.96 [1.52-2.56] |
[PMID 16400609] Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing.
