rs3734353
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs3734353(A;C) |
| Make rs3734353(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 100448693 |
| Gene | SIM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3734353 |
| dbSNP (classic) | rs3734353 |
| ClinGen | rs3734353 |
| ebi | rs3734353 |
| HLI | rs3734353 |
| Exac | rs3734353 |
| Gnomad | rs3734353 |
| Varsome | rs3734353 |
| LitVar | rs3734353 |
| Map | rs3734353 |
| PheGenI | rs3734353 |
| Biobank | rs3734353 |
| 1000 genomes | rs3734353 |
| hgdp | rs3734353 |
| ensembl | rs3734353 |
| geneview | rs3734353 |
| scholar | rs3734353 |
| rs3734353 | |
| pharmgkb | rs3734353 |
| gwascentral | rs3734353 |
| openSNP | rs3734353 |
| 23andMe | rs3734353 |
| SNPshot | rs3734353 |
| SNPdbe | rs3734353 |
| MSV3d | rs3734353 |
| GWAS Ctlg | rs3734353 |
| GMAF | 0.3517 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21512513
] Replication and extension of association between common genetic variants in SIM1 and human adiposity
[PMID 19401419] Common variation in SIM1 is reproducibly associated with BMI in Pima Indians.
| ClinVar | |
|---|---|
| Risk | rs3734353(C;C) |
| Alt | rs3734353(C;C) |
| Reference | Rs3734353(A;A) |
| Significance | Non-pathogenic |
| Disease | Schaaf-yang syndrome |
| Variation | info |
| Gene | SIM1 |
| CLNDBN | Schaaf-yang syndrome |
| Reversed | 1 |
| HGVS | NC_000006.11:g.100896569T>G |
| CLNSRC | |
| CLNACC | RCV000358187.1, |
