rs11236697
From SNPedia
| Orientation | plus |
| Make rs11236697(C;C) |
| Make rs11236697(C;T) |
| Make rs11236697(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 70576391 |
| Gene | SHANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11236697 |
| dbSNP (classic) | rs11236697 |
| ClinGen | rs11236697 |
| ebi | rs11236697 |
| HLI | rs11236697 |
| Exac | rs11236697 |
| Gnomad | rs11236697 |
| Varsome | rs11236697 |
| LitVar | rs11236697 |
| Map | rs11236697 |
| PheGenI | rs11236697 |
| Biobank | rs11236697 |
| 1000 genomes | rs11236697 |
| hgdp | rs11236697 |
| ensembl | rs11236697 |
| geneview | rs11236697 |
| scholar | rs11236697 |
| rs11236697 | |
| pharmgkb | rs11236697 |
| gwascentral | rs11236697 |
| openSNP | rs11236697 |
| 23andMe | rs11236697 |
| SNPshot | rs11236697 |
| SNPdbe | rs11236697 |
| MSV3d | rs11236697 |
| GWAS Ctlg | rs11236697 |
| 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.
