rs892055
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs892055(A;G) |
| Make rs892055(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 38422124 |
| Gene | RASGRP4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs892055 |
| dbSNP (classic) | rs892055 |
| ClinGen | rs892055 |
| ebi | rs892055 |
| HLI | rs892055 |
| Exac | rs892055 |
| Gnomad | rs892055 |
| Varsome | rs892055 |
| LitVar | rs892055 |
| Map | rs892055 |
| PheGenI | rs892055 |
| Biobank | rs892055 |
| 1000 genomes | rs892055 |
| hgdp | rs892055 |
| ensembl | rs892055 |
| geneview | rs892055 |
| scholar | rs892055 |
| rs892055 | |
| pharmgkb | rs892055 |
| gwascentral | rs892055 |
| openSNP | rs892055 |
| 23andMe | rs892055 |
| SNPshot | rs892055 |
| SNPdbe | rs892055 |
| MSV3d | rs892055 |
| GWAS Ctlg | rs892055 |
| GMAF | 0.4894 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21182207 ]
|
| Trait | |
| Title | Variants in several genomic regions associated with Asperger disorder |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | None None |
