rs541299023
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs541299023(A;A) |
| Make rs541299023(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 8013951 |
| Gene | GUCY2D |
| is a | snp |
| is | mentioned by |
| dbSNP | rs541299023 |
| dbSNP (classic) | rs541299023 |
| ClinGen | rs541299023 |
| ebi | rs541299023 |
| HLI | rs541299023 |
| Exac | rs541299023 |
| Gnomad | rs541299023 |
| Varsome | rs541299023 |
| LitVar | rs541299023 |
| Map | rs541299023 |
| PheGenI | rs541299023 |
| Biobank | rs541299023 |
| 1000 genomes | rs541299023 |
| hgdp | rs541299023 |
| ensembl | rs541299023 |
| geneview | rs541299023 |
| scholar | rs541299023 |
| rs541299023 | |
| pharmgkb | rs541299023 |
| gwascentral | rs541299023 |
| openSNP | rs541299023 |
| 23andMe | rs541299023 |
| SNPshot | rs541299023 |
| SNPdbe | rs541299023 |
| MSV3d | rs541299023 |
| GWAS Ctlg | rs541299023 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs541299023(A;A) rs541299023(T;T) |
| Alt | rs541299023(A;A) rs541299023(T;T) |
| Reference | Rs541299023(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GUCY2D |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.7917269G>T |
| CLNSRC | |
| CLNACC | RCV000478042.1, |
