rs56160159
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs56160159(C;T) |
| Make rs56160159(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 5 |
| Position | 56859851 |
| Gene | MAP3K1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56160159 |
| dbSNP (classic) | rs56160159 |
| ClinGen | rs56160159 |
| ebi | rs56160159 |
| HLI | rs56160159 |
| Exac | rs56160159 |
| Gnomad | rs56160159 |
| Varsome | rs56160159 |
| LitVar | rs56160159 |
| Map | rs56160159 |
| PheGenI | rs56160159 |
| Biobank | rs56160159 |
| 1000 genomes | rs56160159 |
| hgdp | rs56160159 |
| ensembl | rs56160159 |
| geneview | rs56160159 |
| scholar | rs56160159 |
| rs56160159 | |
| pharmgkb | rs56160159 |
| gwascentral | rs56160159 |
| openSNP | rs56160159 |
| 23andMe | rs56160159 |
| SNPshot | rs56160159 |
| SNPdbe | rs56160159 |
| MSV3d | rs56160159 |
| GWAS Ctlg | rs56160159 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs56160159(T;T) |
| Alt | rs56160159(T;T) |
| Reference | Rs56160159(C;C) |
| Significance | Probable-Pathogenic |
| Disease | 46 |
| Variation | info |
| Gene | MAP3K1 |
| CLNDBN | 46,XY sex reversal, type 6 |
| Reversed | 0 |
| HGVS | NC_000005.9:g.56155678C>T |
| CLNSRC | |
| CLNACC | RCV000197066.1, |
