rs833497
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs833497(C;C) |
| Make rs833497(C;T) |
| Make rs833497(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 49081890 |
| Gene | DYM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs833497 |
| dbSNP (classic) | rs833497 |
| ClinGen | rs833497 |
| ebi | rs833497 |
| HLI | rs833497 |
| Exac | rs833497 |
| Gnomad | rs833497 |
| Varsome | rs833497 |
| LitVar | rs833497 |
| Map | rs833497 |
| PheGenI | rs833497 |
| Biobank | rs833497 |
| 1000 genomes | rs833497 |
| hgdp | rs833497 |
| ensembl | rs833497 |
| geneview | rs833497 |
| scholar | rs833497 |
| rs833497 | |
| pharmgkb | rs833497 |
| gwascentral | rs833497 |
| openSNP | rs833497 |
| 23andMe | rs833497 |
| SNPshot | rs833497 |
| SNPdbe | rs833497 |
| MSV3d | rs833497 |
| GWAS Ctlg | rs833497 |
| GMAF | 0.2066 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
A recent study in a Japanese population found that each C allele at rs833497 in the DYM gene is associated with 1.16x higher odds of schizophrenia. [PMID 20555340]
Defects in the DYM gene are also associated with Dyggve-Melchior-Clausen syndrome, an extremely rare disease found mostly among families with Lebanese or Spanish ancestry. [PMID 679519] [PMID 17288936]
