rs119484086
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in complete genomics | 
| Make rs119484086(A;A) | 
| Make rs119484086(A;G) | 
| Reference | GRCh38 38.1/142 | 
| Chromosome | 17 | 
| Position | 12992957 | 
| Gene | ELAC2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs119484086 | 
| dbSNP (classic) | rs119484086 | 
| ClinGen | rs119484086 | 
| ebi | rs119484086 | 
| HLI | rs119484086 | 
| Exac | rs119484086 | 
| Gnomad | rs119484086 | 
| Varsome | rs119484086 | 
| LitVar | rs119484086 | 
| Map | rs119484086 | 
| PheGenI | rs119484086 | 
| Biobank | rs119484086 | 
| 1000 genomes | rs119484086 | 
| hgdp | rs119484086 | 
| ensembl | rs119484086 | 
| geneview | rs119484086 | 
| scholar | rs119484086 | 
| rs119484086 | |
| pharmgkb | rs119484086 | 
| gwascentral | rs119484086 | 
| openSNP | rs119484086 | 
| 23andMe | rs119484086 | 
| SNPshot | rs119484086 | 
| SNPdbe | rs119484086 | 
| MSV3d | rs119484086 | 
| GWAS Ctlg | rs119484086 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs119484086(A;A) | 
| Alt | rs119484086(A;A) | 
| Reference | Rs119484086(G;G) | 
| Significance | Pathogenic | 
| Disease | Prostate cancer Combined oxidative phosphorylation deficiency 17 | 
| Variation | info | 
| Gene | ELAC2 | 
| CLNDBN | Prostate cancer, hereditary, 2 Combined oxidative phosphorylation deficiency 17 | 
| Reversed | 1 | 
| HGVS | NC_000017.10:g.12896274C>T | 
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) | 
| CLNACC | RCV000005361.3, RCV000470586.1, | 
