rs919487431
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 4 |
| Position | 155730067 |
| Gene | GUCY1A3, LOC105377506 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs919487431 |
| dbSNP (classic) | rs919487431 |
| ClinGen | rs919487431 |
| ebi | rs919487431 |
| HLI | rs919487431 |
| Exac | rs919487431 |
| Gnomad | rs919487431 |
| Varsome | rs919487431 |
| LitVar | rs919487431 |
| Map | rs919487431 |
| PheGenI | rs919487431 |
| Biobank | rs919487431 |
| 1000 genomes | rs919487431 |
| hgdp | rs919487431 |
| ensembl | rs919487431 |
| geneview | rs919487431 |
| scholar | rs919487431 |
| rs919487431 | |
| pharmgkb | rs919487431 |
| gwascentral | rs919487431 |
| openSNP | rs919487431 |
| 23andMe | rs919487431 |
| SNPshot | rs919487431 |
| SNPdbe | rs919487431 |
| MSV3d | rs919487431 |
| GWAS Ctlg | rs919487431 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs919487431(T;T) |
| Alt | rs919487431(T;T) |
| Reference | Rs919487431(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GUCY1A3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.156651219C>T |
| CLNSRC | |
| CLNACC | RCV000413991.1, |
