rs3495
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs3495(A;A) |
| Make rs3495(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 165773193 |
| Gene | BCHE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3495 |
| dbSNP (classic) | rs3495 |
| ClinGen | rs3495 |
| ebi | rs3495 |
| HLI | rs3495 |
| Exac | rs3495 |
| Gnomad | rs3495 |
| Varsome | rs3495 |
| LitVar | rs3495 |
| Map | rs3495 |
| PheGenI | rs3495 |
| Biobank | rs3495 |
| 1000 genomes | rs3495 |
| hgdp | rs3495 |
| ensembl | rs3495 |
| geneview | rs3495 |
| scholar | rs3495 |
| rs3495 | |
| pharmgkb | rs3495 |
| gwascentral | rs3495 |
| openSNP | rs3495 |
| 23andMe | rs3495 |
| SNPshot | rs3495 |
| SNPdbe | rs3495 |
| MSV3d | rs3495 |
| GWAS Ctlg | rs3495 |
| GMAF | 0.3329 |
| Max Magnitude | 0 |
[PMID 21547979] Variability of the BCHE gene in Amerindians from Paraná, Brazil
| ClinVar | |
|---|---|
| Risk | rs3495(A;A) |
| Alt | rs3495(A;A) |
| Reference | Rs3495(G;G) |
| Significance | Non-pathogenic |
| Disease | Deficiency of butyrylcholine esterase |
| Variation | info |
| Gene | BCHE |
| CLNDBN | Deficiency of butyrylcholine esterase |
| Reversed | 1 |
| HGVS | NC_000003.11:g.165490981C>T |
| CLNSRC | |
| CLNACC | RCV000374138.1, |
