rs165656
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs165656(C;C) |
| Make rs165656(C;G) |
| Make rs165656(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19961340 |
| Gene | COMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs165656 |
| dbSNP (classic) | rs165656 |
| ClinGen | rs165656 |
| ebi | rs165656 |
| HLI | rs165656 |
| Exac | rs165656 |
| Gnomad | rs165656 |
| Varsome | rs165656 |
| LitVar | rs165656 |
| Map | rs165656 |
| PheGenI | rs165656 |
| Biobank | rs165656 |
| 1000 genomes | rs165656 |
| hgdp | rs165656 |
| ensembl | rs165656 |
| geneview | rs165656 |
| scholar | rs165656 |
| rs165656 | |
| pharmgkb | rs165656 |
| gwascentral | rs165656 |
| openSNP | rs165656 |
| 23andMe | rs165656 |
| SNPshot | rs165656 |
| SNPdbe | rs165656 |
| MSV3d | rs165656 |
| GWAS Ctlg | rs165656 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23446089] Catechol-O-methyltransferase (COMT) gene polymorphisms as risk factor in temporomandibular disorders patients from Southern Italy
