rs745683775
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs745683775(C;G) |
| Make rs745683775(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 46560448 |
| Gene | LOXHD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs745683775 |
| dbSNP (classic) | rs745683775 |
| ClinGen | rs745683775 |
| ebi | rs745683775 |
| HLI | rs745683775 |
| Exac | rs745683775 |
| Gnomad | rs745683775 |
| Varsome | rs745683775 |
| LitVar | rs745683775 |
| Map | rs745683775 |
| PheGenI | rs745683775 |
| Biobank | rs745683775 |
| 1000 genomes | rs745683775 |
| hgdp | rs745683775 |
| ensembl | rs745683775 |
| geneview | rs745683775 |
| scholar | rs745683775 |
| rs745683775 | |
| pharmgkb | rs745683775 |
| gwascentral | rs745683775 |
| openSNP | rs745683775 |
| 23andMe | rs745683775 |
| SNPshot | rs745683775 |
| SNPdbe | rs745683775 |
| MSV3d | rs745683775 |
| GWAS Ctlg | rs745683775 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs745683775(G;G) rs745683775(T;T) |
| Alt | rs745683775(G;G) rs745683775(T;T) |
| Reference | Rs745683775(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | LOXHD1 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.44140411C>G |
| CLNSRC | |
| CLNACC | RCV000219519.1, RCV000485022.1, |
