rs149150736
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs149150736(C;T) | 
| Make rs149150736(T;T) | 
| Reference | GRCh38.p2 38.2/146 | 
| Chromosome | 10 | 
| Position | 97611582 | 
| Gene | HOGA1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs149150736 | 
| dbSNP (classic) | rs149150736 | 
| ClinGen | rs149150736 | 
| ebi | rs149150736 | 
| HLI | rs149150736 | 
| Exac | rs149150736 | 
| Gnomad | rs149150736 | 
| Varsome | rs149150736 | 
| LitVar | rs149150736 | 
| Map | rs149150736 | 
| PheGenI | rs149150736 | 
| Biobank | rs149150736 | 
| 1000 genomes | rs149150736 | 
| hgdp | rs149150736 | 
| ensembl | rs149150736 | 
| geneview | rs149150736 | 
| scholar | rs149150736 | 
| rs149150736 | |
| pharmgkb | rs149150736 | 
| gwascentral | rs149150736 | 
| openSNP | rs149150736 | 
| 23andMe | rs149150736 | 
| SNPshot | rs149150736 | 
| SNPdbe | rs149150736 | 
| MSV3d | rs149150736 | 
| GWAS Ctlg | rs149150736 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs149150736(T;T) | 
| Alt | rs149150736(T;T) | 
| Reference | Rs149150736(C;C) | 
| Significance | Pathogenic | 
| Disease | Primary hyperoxaluria | 
| Variation | info | 
| Gene | HOGA1 | 
| CLNDBN | Primary hyperoxaluria, type III | 
| Reversed | 0 | 
| HGVS | NC_000010.10:g.99371339C>T | 
| CLNSRC | |
| CLNACC | RCV000186486.1, | 
