rs3745635
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs3745635(A;A) |
| Make rs3745635(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 5844332 |
| Gene | FUT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3745635 |
| dbSNP (classic) | rs3745635 |
| ClinGen | rs3745635 |
| ebi | rs3745635 |
| HLI | rs3745635 |
| Exac | rs3745635 |
| Gnomad | rs3745635 |
| Varsome | rs3745635 |
| LitVar | rs3745635 |
| Map | rs3745635 |
| PheGenI | rs3745635 |
| Biobank | rs3745635 |
| 1000 genomes | rs3745635 |
| hgdp | rs3745635 |
| ensembl | rs3745635 |
| geneview | rs3745635 |
| scholar | rs3745635 |
| rs3745635 | |
| pharmgkb | rs3745635 |
| gwascentral | rs3745635 |
| openSNP | rs3745635 |
| 23andMe | rs3745635 |
| SNPshot | rs3745635 |
| SNPdbe | rs3745635 |
| MSV3d | rs3745635 |
| GWAS Ctlg | rs3745635 |
| GMAF | 0.1382 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs3745635(A;A) |
| Alt | rs3745635(A;A) |
| Reference | Rs3745635(G;G) |
| Significance | Other |
| Disease | Le(-) PHENOTYPE |
| Variation | info |
| Gene | FUT3 |
| CLNDBN | Le(-) PHENOTYPE |
| Reversed | 1 |
| HGVS | NC_000019.9:g.5844343C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019289.23, |
