rs16996652
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs16996652(A;T) |
| Make rs16996652(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 36300203 |
| Gene | MYH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16996652 |
| dbSNP (classic) | rs16996652 |
| ClinGen | rs16996652 |
| ebi | rs16996652 |
| HLI | rs16996652 |
| Exac | rs16996652 |
| Gnomad | rs16996652 |
| Varsome | rs16996652 |
| LitVar | rs16996652 |
| Map | rs16996652 |
| PheGenI | rs16996652 |
| Biobank | rs16996652 |
| 1000 genomes | rs16996652 |
| hgdp | rs16996652 |
| ensembl | rs16996652 |
| geneview | rs16996652 |
| scholar | rs16996652 |
| rs16996652 | |
| pharmgkb | rs16996652 |
| gwascentral | rs16996652 |
| openSNP | rs16996652 |
| 23andMe | rs16996652 |
| SNPshot | rs16996652 |
| SNPdbe | rs16996652 |
| MSV3d | rs16996652 |
| GWAS Ctlg | rs16996652 |
| Max Magnitude | 0 |
[PMID 19891592] Association Among Polymorphisms at MYH9, Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China
| ClinVar | |
|---|---|
| Risk | rs16996652(T;T) |
| Alt | rs16996652(T;T) |
| Reference | Rs16996652(A;A) |
| Significance | Non-pathogenic |
| Disease | MYH9 related disorders |
| Variation | info |
| Gene | MYH9 |
| CLNDBN | MYH9 related disorders |
| Reversed | 0 |
| HGVS | NC_000022.10:g.36696249A>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000032219.1, |
