rs864622060
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common genotype |
| Make rs864622060(C;C) |
| Make rs864622060(C;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 9 |
| Position | 136505776 |
| Gene | NOTCH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs864622060 |
| dbSNP (classic) | rs864622060 |
| ClinGen | rs864622060 |
| ebi | rs864622060 |
| HLI | rs864622060 |
| Exac | rs864622060 |
| Gnomad | rs864622060 |
| Varsome | rs864622060 |
| LitVar | rs864622060 |
| Map | rs864622060 |
| PheGenI | rs864622060 |
| Biobank | rs864622060 |
| 1000 genomes | rs864622060 |
| hgdp | rs864622060 |
| ensembl | rs864622060 |
| geneview | rs864622060 |
| scholar | rs864622060 |
| rs864622060 | |
| pharmgkb | rs864622060 |
| gwascentral | rs864622060 |
| openSNP | rs864622060 |
| 23andMe | rs864622060 |
| SNPshot | rs864622060 |
| SNPdbe | rs864622060 |
| MSV3d | rs864622060 |
| GWAS Ctlg | rs864622060 |
| Max Magnitude | 0 |
aka NM_017617.4(NOTCH1):c.4120T>C or (p.Cys1374Arg)
OMIM pathogenic variant
