rs74336682
From SNPedia
| Orientation | plus |
| Make rs74336682(A;A) |
| Make rs74336682(A;G) |
| Make rs74336682(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 70586855 |
| Gene | SHANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs74336682 |
| dbSNP (classic) | rs74336682 |
| ClinGen | rs74336682 |
| ebi | rs74336682 |
| HLI | rs74336682 |
| Exac | rs74336682 |
| Gnomad | rs74336682 |
| Varsome | rs74336682 |
| LitVar | rs74336682 |
| Map | rs74336682 |
| PheGenI | rs74336682 |
| Biobank | rs74336682 |
| 1000 genomes | rs74336682 |
| hgdp | rs74336682 |
| ensembl | rs74336682 |
| geneview | rs74336682 |
| scholar | rs74336682 |
| rs74336682 | |
| pharmgkb | rs74336682 |
| gwascentral | rs74336682 |
| openSNP | rs74336682 |
| 23andMe | rs74336682 |
| SNPshot | rs74336682 |
| SNPdbe | rs74336682 |
| MSV3d | rs74336682 |
| GWAS Ctlg | rs74336682 |
| 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.
