rs753151497
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs753151497(C;C) |
| Make rs753151497(C;T) |
| Make rs753151497(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 1 |
| Position | 25566928 |
| Gene | LDLRAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753151497 |
| dbSNP (classic) | rs753151497 |
| ClinGen | rs753151497 |
| ebi | rs753151497 |
| HLI | rs753151497 |
| Exac | rs753151497 |
| Gnomad | rs753151497 |
| Varsome | rs753151497 |
| LitVar | rs753151497 |
| Map | rs753151497 |
| PheGenI | rs753151497 |
| Biobank | rs753151497 |
| 1000 genomes | rs753151497 |
| hgdp | rs753151497 |
| ensembl | rs753151497 |
| geneview | rs753151497 |
| scholar | rs753151497 |
| rs753151497 | |
| pharmgkb | rs753151497 |
| gwascentral | rs753151497 |
| openSNP | rs753151497 |
| 23andMe | rs753151497 |
| SNPshot | rs753151497 |
| SNPdbe | rs753151497 |
| MSV3d | rs753151497 |
| GWAS Ctlg | rs753151497 |
| Max Magnitude | 0 |
aka NM_015627.2(LDLRAP1):c.863C>T or (p.Ser288Leu)
OMIM pathogenic variant
