rs377731205
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs377731205(C;T) |
| Make rs377731205(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 19 |
| Position | 36097074 |
| Gene | WDR62 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs377731205 |
| dbSNP (classic) | rs377731205 |
| ClinGen | rs377731205 |
| ebi | rs377731205 |
| HLI | rs377731205 |
| Exac | rs377731205 |
| Gnomad | rs377731205 |
| Varsome | rs377731205 |
| LitVar | rs377731205 |
| Map | rs377731205 |
| PheGenI | rs377731205 |
| Biobank | rs377731205 |
| 1000 genomes | rs377731205 |
| hgdp | rs377731205 |
| ensembl | rs377731205 |
| geneview | rs377731205 |
| scholar | rs377731205 |
| rs377731205 | |
| pharmgkb | rs377731205 |
| gwascentral | rs377731205 |
| openSNP | rs377731205 |
| 23andMe | rs377731205 |
| SNPshot | rs377731205 |
| SNPdbe | rs377731205 |
| MSV3d | rs377731205 |
| GWAS Ctlg | rs377731205 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs377731205(T;T) |
| Alt | rs377731205(T;T) |
| Reference | Rs377731205(C;C) |
| Significance | Pathogenic |
| Disease | Abnormality of neuronal migration |
| Variation | info |
| Gene | WDR62 |
| CLNDBN | Abnormality of neuronal migration |
| Reversed | 0 |
| HGVS | NC_000019.9:g.36587976C>T |
| CLNSRC | |
| CLNACC | RCV000201333.1, |
