rs1130496
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1130496(A;A) |
| Make rs1130496(A;G) |
| Make rs1130496(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 158167203 |
| Gene | PTPRN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1130496 |
| dbSNP (classic) | rs1130496 |
| ClinGen | rs1130496 |
| ebi | rs1130496 |
| HLI | rs1130496 |
| Exac | rs1130496 |
| Gnomad | rs1130496 |
| Varsome | rs1130496 |
| LitVar | rs1130496 |
| Map | rs1130496 |
| PheGenI | rs1130496 |
| Biobank | rs1130496 |
| 1000 genomes | rs1130496 |
| hgdp | rs1130496 |
| ensembl | rs1130496 |
| geneview | rs1130496 |
| scholar | rs1130496 |
| rs1130496 | |
| pharmgkb | rs1130496 |
| gwascentral | rs1130496 |
| openSNP | rs1130496 |
| 23andMe | rs1130496 |
| SNPshot | rs1130496 |
| SNPdbe | rs1130496 |
| MSV3d | rs1130496 |
| GWAS Ctlg | rs1130496 |
| GMAF | 0.3526 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19456320
] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
