rs739097
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs739097(A;A) |
| Make rs739097(A;G) |
| Make rs739097(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36350034 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs739097 |
| dbSNP (classic) | rs739097 |
| ClinGen | rs739097 |
| ebi | rs739097 |
| HLI | rs739097 |
| Exac | rs739097 |
| Gnomad | rs739097 |
| Varsome | rs739097 |
| LitVar | rs739097 |
| Map | rs739097 |
| PheGenI | rs739097 |
| Biobank | rs739097 |
| 1000 genomes | rs739097 |
| hgdp | rs739097 |
| ensembl | rs739097 |
| geneview | rs739097 |
| scholar | rs739097 |
| rs739097 | |
| pharmgkb | rs739097 |
| gwascentral | rs739097 |
| openSNP | rs739097 |
| 23andMe | rs739097 |
| SNPshot | rs739097 |
| SNPdbe | rs739097 |
| MSV3d | rs739097 |
| GWAS Ctlg | rs739097 |
| GMAF | 0.4949 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 19320731] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
[PMID 18571626] RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
[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.
