rs149615348
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs149615348(A;A) |
| Make rs149615348(A;G) |
| Make rs149615348(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 84867039 |
| Gene | CRISPLD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149615348 |
| dbSNP (classic) | rs149615348 |
| ClinGen | rs149615348 |
| ebi | rs149615348 |
| HLI | rs149615348 |
| Exac | rs149615348 |
| Gnomad | rs149615348 |
| Varsome | rs149615348 |
| LitVar | rs149615348 |
| Map | rs149615348 |
| PheGenI | rs149615348 |
| Biobank | rs149615348 |
| 1000 genomes | rs149615348 |
| hgdp | rs149615348 |
| ensembl | rs149615348 |
| geneview | rs149615348 |
| scholar | rs149615348 |
| rs149615348 | |
| pharmgkb | rs149615348 |
| gwascentral | rs149615348 |
| openSNP | rs149615348 |
| 23andMe | rs149615348 |
| SNPshot | rs149615348 |
| SNPdbe | rs149615348 |
| MSV3d | rs149615348 |
| GWAS Ctlg | rs149615348 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
