rs7170637
From SNPedia
| Orientation | minus |
| Stabilized | plus |
| Make rs7170637(A;A) |
| Make rs7170637(A;G) |
| Make rs7170637(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 22903836 |
| Gene | CYFIP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7170637 |
| dbSNP (classic) | rs7170637 |
| ClinGen | rs7170637 |
| ebi | rs7170637 |
| HLI | rs7170637 |
| Exac | rs7170637 |
| Gnomad | rs7170637 |
| Varsome | rs7170637 |
| LitVar | rs7170637 |
| Map | rs7170637 |
| PheGenI | rs7170637 |
| Biobank | rs7170637 |
| 1000 genomes | rs7170637 |
| hgdp | rs7170637 |
| ensembl | rs7170637 |
| geneview | rs7170637 |
| scholar | rs7170637 |
| rs7170637 | |
| pharmgkb | rs7170637 |
| gwascentral | rs7170637 |
| openSNP | rs7170637 |
| 23andMe | rs7170637 |
| SNPshot | rs7170637 |
| SNPdbe | rs7170637 |
| MSV3d | rs7170637 |
| GWAS Ctlg | rs7170637 |
| Max Magnitude | 0 |
[PMID 24442360] Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
