rs775225727
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs775225727(A;A) |
| Make rs775225727(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 7 |
| Position | 69599802 |
| Gene | AUTS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs775225727 |
| dbSNP (classic) | rs775225727 |
| ClinGen | rs775225727 |
| ebi | rs775225727 |
| HLI | rs775225727 |
| Exac | rs775225727 |
| Gnomad | rs775225727 |
| Varsome | rs775225727 |
| LitVar | rs775225727 |
| Map | rs775225727 |
| PheGenI | rs775225727 |
| Biobank | rs775225727 |
| 1000 genomes | rs775225727 |
| hgdp | rs775225727 |
| ensembl | rs775225727 |
| geneview | rs775225727 |
| scholar | rs775225727 |
| rs775225727 | |
| pharmgkb | rs775225727 |
| gwascentral | rs775225727 |
| openSNP | rs775225727 |
| 23andMe | rs775225727 |
| SNPshot | rs775225727 |
| SNPdbe | rs775225727 |
| MSV3d | rs775225727 |
| GWAS Ctlg | rs775225727 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs775225727(A;A) rs775225727(G;G) |
| Alt | rs775225727(A;A) rs775225727(G;G) |
| Reference | Rs775225727(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AUTS2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000007.13:g.69064788C>A |
| CLNSRC | |
| CLNACC | RCV000440958.1, |
