rs112892337
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs112892337(C;C) |
| Make rs112892337(C;G) |
| Make rs112892337(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 8 |
| Position | 134602310 |
| Gene | ZFAT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112892337 |
| dbSNP (classic) | rs112892337 |
| ClinGen | rs112892337 |
| ebi | rs112892337 |
| HLI | rs112892337 |
| Exac | rs112892337 |
| Gnomad | rs112892337 |
| Varsome | rs112892337 |
| LitVar | rs112892337 |
| Map | rs112892337 |
| PheGenI | rs112892337 |
| Biobank | rs112892337 |
| 1000 genomes | rs112892337 |
| hgdp | rs112892337 |
| ensembl | rs112892337 |
| geneview | rs112892337 |
| scholar | rs112892337 |
| rs112892337 | |
| pharmgkb | rs112892337 |
| gwascentral | rs112892337 |
| openSNP | rs112892337 |
| 23andMe | rs112892337 |
| SNPshot | rs112892337 |
| SNPdbe | rs112892337 |
| MSV3d | rs112892337 |
| GWAS Ctlg | rs112892337 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
| ClinVar | |
|---|---|
| Risk | rs112892337(C;C) |
| Alt | rs112892337(C;C) |
| Reference | rs112892337(G;G) |
| Significance | Unknown |
| Disease | not specified |
| Variation | info |
| Gene | ZFAT |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000008.10:g.135614553G>C |
| CLNSRC | |
| CLNACC | RCV000455390.1, |
