rs1017700992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 12 |
| Position | 53314796 |
| Gene | AAAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1017700992 |
| dbSNP (classic) | rs1017700992 |
| ClinGen | rs1017700992 |
| ebi | rs1017700992 |
| HLI | rs1017700992 |
| Exac | rs1017700992 |
| Gnomad | rs1017700992 |
| Varsome | rs1017700992 |
| LitVar | rs1017700992 |
| Map | rs1017700992 |
| PheGenI | rs1017700992 |
| Biobank | rs1017700992 |
| 1000 genomes | rs1017700992 |
| hgdp | rs1017700992 |
| ensembl | rs1017700992 |
| geneview | rs1017700992 |
| scholar | rs1017700992 |
| rs1017700992 | |
| pharmgkb | rs1017700992 |
| gwascentral | rs1017700992 |
| openSNP | rs1017700992 |
| 23andMe | rs1017700992 |
| SNPshot | rs1017700992 |
| SNPdbe | rs1017700992 |
| MSV3d | rs1017700992 |
| GWAS Ctlg | rs1017700992 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1017700992(A;A) |
| Alt | rs1017700992(A;A) |
| Reference | Rs1017700992(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AAAS |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000012.11:g.53708580G>T |
| CLNSRC | |
| CLNACC | RCV000413311.1, |
