rs796051935
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in clinvar | 
| Make rs796051935(A;A) | 
| Make rs796051935(A;G) | 
| Reference | GRCh38.p2 38.2/146 | 
| Chromosome | 9 | 
| Position | 130464132 | 
| Gene | ASS1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs796051935 | 
| dbSNP (classic) | rs796051935 | 
| ClinGen | rs796051935 | 
| ebi | rs796051935 | 
| HLI | rs796051935 | 
| Exac | rs796051935 | 
| Gnomad | rs796051935 | 
| Varsome | rs796051935 | 
| LitVar | rs796051935 | 
| Map | rs796051935 | 
| PheGenI | rs796051935 | 
| Biobank | rs796051935 | 
| 1000 genomes | rs796051935 | 
| hgdp | rs796051935 | 
| ensembl | rs796051935 | 
| geneview | rs796051935 | 
| scholar | rs796051935 | 
| rs796051935 | |
| pharmgkb | rs796051935 | 
| gwascentral | rs796051935 | 
| openSNP | rs796051935 | 
| 23andMe | rs796051935 | 
| SNPshot | rs796051935 | 
| SNPdbe | rs796051935 | 
| MSV3d | rs796051935 | 
| GWAS Ctlg | rs796051935 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs796051935(A;A) | 
| Alt | rs796051935(A;A) | 
| Reference | Rs796051935(G;G) | 
| Significance | Probable-Pathogenic | 
| Disease | not provided | 
| Variation | info | 
| Gene | ASS1 | 
| CLNDBN | not provided | 
| Reversed | 0 | 
| HGVS | NC_000009.11:g.133339519G>A | 
| CLNSRC | |
| CLNACC | RCV000185793.1, | 


