rs1450425
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 0.5 | benign most likely |
| (G;G) | 0.5 | benign most likely |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 18 |
| Position | 46529070 |
| Gene | LOXHD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1450425 |
| dbSNP (classic) | rs1450425 |
| ClinGen | rs1450425 |
| ebi | rs1450425 |
| HLI | rs1450425 |
| Exac | rs1450425 |
| Gnomad | rs1450425 |
| Varsome | rs1450425 |
| LitVar | rs1450425 |
| Map | rs1450425 |
| PheGenI | rs1450425 |
| Biobank | rs1450425 |
| 1000 genomes | rs1450425 |
| hgdp | rs1450425 |
| ensembl | rs1450425 |
| geneview | rs1450425 |
| scholar | rs1450425 |
| rs1450425 | |
| pharmgkb | rs1450425 |
| gwascentral | rs1450425 |
| openSNP | rs1450425 |
| 23andMe | rs1450425 |
| SNPshot | rs1450425 |
| SNPdbe | rs1450425 |
| MSV3d | rs1450425 |
| GWAS Ctlg | rs1450425 |
| Max Magnitude | 0.5 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | Rs1450425(G;G) |
| Alt | Rs1450425(G;G) |
| Reference | Rs1450425(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | LOXHD1 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000018.9:g.44109033T>C |
| CLNSRC | |
| CLNACC | RCV000171270.2, |
[PMID 27242896
] Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.
