rs141476300
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs141476300(A;A) |
| Make rs141476300(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 45979728 |
| Gene | FYCO1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141476300 |
| dbSNP (classic) | rs141476300 |
| ClinGen | rs141476300 |
| ebi | rs141476300 |
| HLI | rs141476300 |
| Exac | rs141476300 |
| Gnomad | rs141476300 |
| Varsome | rs141476300 |
| LitVar | rs141476300 |
| Map | rs141476300 |
| PheGenI | rs141476300 |
| Biobank | rs141476300 |
| 1000 genomes | rs141476300 |
| hgdp | rs141476300 |
| ensembl | rs141476300 |
| geneview | rs141476300 |
| scholar | rs141476300 |
| rs141476300 | |
| pharmgkb | rs141476300 |
| gwascentral | rs141476300 |
| openSNP | rs141476300 |
| 23andMe | rs141476300 |
| SNPshot | rs141476300 |
| SNPdbe | rs141476300 |
| MSV3d | rs141476300 |
| GWAS Ctlg | rs141476300 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs141476300(A;A) |
| Alt | rs141476300(A;A) |
| Reference | Rs141476300(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FYCO1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.46021220G>A |
| CLNSRC | |
| CLNACC | RCV000488185.1, |
