rs149956316
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs149956316(A;A) |
| Make rs149956316(A;G) |
| Make rs149956316(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | X |
| Position | 110706284 |
| Gene | CHRDL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149956316 |
| dbSNP (classic) | rs149956316 |
| ClinGen | rs149956316 |
| ebi | rs149956316 |
| HLI | rs149956316 |
| Exac | rs149956316 |
| Gnomad | rs149956316 |
| Varsome | rs149956316 |
| LitVar | rs149956316 |
| Map | rs149956316 |
| PheGenI | rs149956316 |
| Biobank | rs149956316 |
| 1000 genomes | rs149956316 |
| hgdp | rs149956316 |
| ensembl | rs149956316 |
| geneview | rs149956316 |
| scholar | rs149956316 |
| rs149956316 | |
| pharmgkb | rs149956316 |
| gwascentral | rs149956316 |
| openSNP | rs149956316 |
| 23andMe | rs149956316 |
| SNPshot | rs149956316 |
| SNPdbe | rs149956316 |
| MSV3d | rs149956316 |
| GWAS Ctlg | rs149956316 |
| Max Magnitude | 0 |
[PMID 25093588
] Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness
