rs149032771
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs149032771(A;A) |
| Make rs149032771(A;G) |
| Make rs149032771(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 7 |
| Position | 147300272 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149032771 |
| dbSNP (classic) | rs149032771 |
| ClinGen | rs149032771 |
| ebi | rs149032771 |
| HLI | rs149032771 |
| Exac | rs149032771 |
| Gnomad | rs149032771 |
| Varsome | rs149032771 |
| LitVar | rs149032771 |
| Map | rs149032771 |
| PheGenI | rs149032771 |
| Biobank | rs149032771 |
| 1000 genomes | rs149032771 |
| hgdp | rs149032771 |
| ensembl | rs149032771 |
| geneview | rs149032771 |
| scholar | rs149032771 |
| rs149032771 | |
| pharmgkb | rs149032771 |
| gwascentral | rs149032771 |
| openSNP | rs149032771 |
| 23andMe | rs149032771 |
| SNPshot | rs149032771 |
| SNPdbe | rs149032771 |
| MSV3d | rs149032771 |
| GWAS Ctlg | rs149032771 |
| Max Magnitude | 0 |
OMIM pathogenic variant
