rs75357229
From SNPedia
| Orientation | plus |
| Make rs75357229(C;C) |
| Make rs75357229(C;T) |
| Make rs75357229(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 71164647 |
| Gene | SHANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75357229 |
| dbSNP (classic) | rs75357229 |
| ClinGen | rs75357229 |
| ebi | rs75357229 |
| HLI | rs75357229 |
| Exac | rs75357229 |
| Gnomad | rs75357229 |
| Varsome | rs75357229 |
| LitVar | rs75357229 |
| Map | rs75357229 |
| PheGenI | rs75357229 |
| Biobank | rs75357229 |
| 1000 genomes | rs75357229 |
| hgdp | rs75357229 |
| ensembl | rs75357229 |
| geneview | rs75357229 |
| scholar | rs75357229 |
| rs75357229 | |
| pharmgkb | rs75357229 |
| gwascentral | rs75357229 |
| openSNP | rs75357229 |
| 23andMe | rs75357229 |
| SNPshot | rs75357229 |
| SNPdbe | rs75357229 |
| MSV3d | rs75357229 |
| GWAS Ctlg | rs75357229 |
| Max Magnitude | 0 |
[PMID 30629339] SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
