rs121918385
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;G) | 3 | Carrier of a hypobetalipoproteinemia mutation |
| (G;G) | 0 | common in clinvar |
| Make rs121918385(-;-) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 21003241 |
| Gene | APOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121918385 |
| dbSNP (classic) | rs121918385 |
| ClinGen | rs121918385 |
| ebi | rs121918385 |
| HLI | rs121918385 |
| Exac | rs121918385 |
| Gnomad | rs121918385 |
| Varsome | rs121918385 |
| LitVar | rs121918385 |
| Map | rs121918385 |
| PheGenI | rs121918385 |
| Biobank | rs121918385 |
| 1000 genomes | rs121918385 |
| hgdp | rs121918385 |
| ensembl | rs121918385 |
| geneview | rs121918385 |
| scholar | rs121918385 |
| rs121918385 | |
| pharmgkb | rs121918385 |
| gwascentral | rs121918385 |
| openSNP | rs121918385 |
| 23andMe | rs121918385 |
| SNPshot | rs121918385 |
| SNPdbe | rs121918385 |
| MSV3d | rs121918385 |
| GWAS Ctlg | rs121918385 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs121918385(-;-) |
| Alt | rs121918385(-;-) |
| Reference | Rs121918385(G;G) |
| Significance | Pathogenic |
| Disease | Familial hypobetalipoproteinemia |
| Variation | info |
| Gene | APOB |
| CLNDBN | Familial hypobetalipoproteinemia |
| Reversed | 1 |
| HGVS | NC_000002.11:g.21226113delC |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019474.26, |
