rs6661174
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs6661174(C;C) |
| Make rs6661174(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 171208951 |
| Gene | FMO2, LOC105371611 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6661174 |
| dbSNP (classic) | rs6661174 |
| ClinGen | rs6661174 |
| ebi | rs6661174 |
| HLI | rs6661174 |
| Exac | rs6661174 |
| Gnomad | rs6661174 |
| Varsome | rs6661174 |
| LitVar | rs6661174 |
| Map | rs6661174 |
| PheGenI | rs6661174 |
| Biobank | rs6661174 |
| 1000 genomes | rs6661174 |
| hgdp | rs6661174 |
| ensembl | rs6661174 |
| geneview | rs6661174 |
| scholar | rs6661174 |
| rs6661174 | |
| pharmgkb | rs6661174 |
| gwascentral | rs6661174 |
| openSNP | rs6661174 |
| 23andMe | rs6661174 |
| SNPshot | rs6661174 |
| SNPdbe | rs6661174 |
| MSV3d | rs6661174 |
| GWAS Ctlg | rs6661174 |
| GMAF | 0.03535 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19200524
] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.
[PMID 19420133] Characterization of sulfoxygenation and structural implications of human flavin-containing monooxygenase isoform 2 (FMO2.1) variants S195L and N413K.
[PMID 21205862] Gene inactivation and its implications for annotation in the era of personal genomics.
