rs3764628
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs3764628(A;A) |
| Make rs3764628(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 18636795 |
| Gene | KLHL26 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3764628 |
| dbSNP (classic) | rs3764628 |
| ClinGen | rs3764628 |
| ebi | rs3764628 |
| HLI | rs3764628 |
| Exac | rs3764628 |
| Gnomad | rs3764628 |
| Varsome | rs3764628 |
| LitVar | rs3764628 |
| Map | rs3764628 |
| PheGenI | rs3764628 |
| Biobank | rs3764628 |
| 1000 genomes | rs3764628 |
| hgdp | rs3764628 |
| ensembl | rs3764628 |
| geneview | rs3764628 |
| scholar | rs3764628 |
| rs3764628 | |
| pharmgkb | rs3764628 |
| gwascentral | rs3764628 |
| openSNP | rs3764628 |
| 23andMe | rs3764628 |
| SNPshot | rs3764628 |
| SNPdbe | rs3764628 |
| MSV3d | rs3764628 |
| GWAS Ctlg | rs3764628 |
| GMAF | 0.09275 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22419666 ]
|
| Trait | |
| Title | Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | 1.8900 None |
