rs757966746
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs757966746(A;A) |
| Make rs757966746(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 34294083 |
| Gene | AHCY |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757966746 |
| dbSNP (classic) | rs757966746 |
| ClinGen | rs757966746 |
| ebi | rs757966746 |
| HLI | rs757966746 |
| Exac | rs757966746 |
| Gnomad | rs757966746 |
| Varsome | rs757966746 |
| LitVar | rs757966746 |
| Map | rs757966746 |
| PheGenI | rs757966746 |
| Biobank | rs757966746 |
| 1000 genomes | rs757966746 |
| hgdp | rs757966746 |
| ensembl | rs757966746 |
| geneview | rs757966746 |
| scholar | rs757966746 |
| rs757966746 | |
| pharmgkb | rs757966746 |
| gwascentral | rs757966746 |
| openSNP | rs757966746 |
| 23andMe | rs757966746 |
| SNPshot | rs757966746 |
| SNPdbe | rs757966746 |
| MSV3d | rs757966746 |
| GWAS Ctlg | rs757966746 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757966746(A;A) |
| Alt | rs757966746(A;A) |
| Reference | Rs757966746(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AHCY |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000020.10:g.32881889G>A |
| CLNSRC | |
| CLNACC | RCV000223995.1, |
