rs757778790
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs757778790(A;A) |
| Make rs757778790(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 14 |
| Position | 75633674 |
| Gene | FLVCR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757778790 |
| dbSNP (classic) | rs757778790 |
| ClinGen | rs757778790 |
| ebi | rs757778790 |
| HLI | rs757778790 |
| Exac | rs757778790 |
| Gnomad | rs757778790 |
| Varsome | rs757778790 |
| LitVar | rs757778790 |
| Map | rs757778790 |
| PheGenI | rs757778790 |
| Biobank | rs757778790 |
| 1000 genomes | rs757778790 |
| hgdp | rs757778790 |
| ensembl | rs757778790 |
| geneview | rs757778790 |
| scholar | rs757778790 |
| rs757778790 | |
| pharmgkb | rs757778790 |
| gwascentral | rs757778790 |
| openSNP | rs757778790 |
| 23andMe | rs757778790 |
| SNPshot | rs757778790 |
| SNPdbe | rs757778790 |
| MSV3d | rs757778790 |
| GWAS Ctlg | rs757778790 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757778790(A;A) |
| Alt | rs757778790(A;A) |
| Reference | Rs757778790(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FLVCR2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.76100017G>A |
| CLNSRC | |
| CLNACC | RCV000171224.1, |
