rs2071731
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2071731(A;A) |
| Make rs2071731(A;G) |
| Make rs2071731(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36322813 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2071731 |
| dbSNP (classic) | rs2071731 |
| ClinGen | rs2071731 |
| ebi | rs2071731 |
| HLI | rs2071731 |
| Exac | rs2071731 |
| Gnomad | rs2071731 |
| Varsome | rs2071731 |
| LitVar | rs2071731 |
| Map | rs2071731 |
| PheGenI | rs2071731 |
| Biobank | rs2071731 |
| 1000 genomes | rs2071731 |
| hgdp | rs2071731 |
| ensembl | rs2071731 |
| geneview | rs2071731 |
| scholar | rs2071731 |
| rs2071731 | |
| pharmgkb | rs2071731 |
| gwascentral | rs2071731 |
| openSNP | rs2071731 |
| 23andMe | rs2071731 |
| SNPshot | rs2071731 |
| SNPdbe | rs2071731 |
| MSV3d | rs2071731 |
| GWAS Ctlg | rs2071731 |
| GMAF | 0.4233 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19320731] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
[PMID 18716610
] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
[PMID 20124285] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
