rs371642222
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs371642222(C;C) |
| Make rs371642222(C;T) |
| Make rs371642222(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 7 |
| Position | 148217323 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371642222 |
| dbSNP (classic) | rs371642222 |
| ClinGen | rs371642222 |
| ebi | rs371642222 |
| HLI | rs371642222 |
| Exac | rs371642222 |
| Gnomad | rs371642222 |
| Varsome | rs371642222 |
| LitVar | rs371642222 |
| Map | rs371642222 |
| PheGenI | rs371642222 |
| Biobank | rs371642222 |
| 1000 genomes | rs371642222 |
| hgdp | rs371642222 |
| ensembl | rs371642222 |
| geneview | rs371642222 |
| scholar | rs371642222 |
| rs371642222 | |
| pharmgkb | rs371642222 |
| gwascentral | rs371642222 |
| openSNP | rs371642222 |
| 23andMe | rs371642222 |
| SNPshot | rs371642222 |
| SNPdbe | rs371642222 |
| MSV3d | rs371642222 |
| GWAS Ctlg | rs371642222 |
| Max Magnitude | 0 |
aka NM_014141.5(CNTNAP2):c.3046C>T or (p.Arg1016Ter)
OMIM pathogenic variant
