rs148360332
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs148360332(C;T) | 
| Make rs148360332(T;T) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 14 | 
| Position | 77453359 | 
| Gene | VIPAS39 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs148360332 | 
| dbSNP (classic) | rs148360332 | 
| ClinGen | rs148360332 | 
| ebi | rs148360332 | 
| HLI | rs148360332 | 
| Exac | rs148360332 | 
| Gnomad | rs148360332 | 
| Varsome | rs148360332 | 
| LitVar | rs148360332 | 
| Map | rs148360332 | 
| PheGenI | rs148360332 | 
| Biobank | rs148360332 | 
| 1000 genomes | rs148360332 | 
| hgdp | rs148360332 | 
| ensembl | rs148360332 | 
| geneview | rs148360332 | 
| scholar | rs148360332 | 
| rs148360332 | |
| pharmgkb | rs148360332 | 
| gwascentral | rs148360332 | 
| openSNP | rs148360332 | 
| 23andMe | rs148360332 | 
| SNPshot | rs148360332 | 
| SNPdbe | rs148360332 | 
| MSV3d | rs148360332 | 
| GWAS Ctlg | rs148360332 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs148360332(T;T) | 
| Alt | rs148360332(T;T) | 
| Reference | Rs148360332(C;C) | 
| Significance | Other | 
| Disease | not specified | 
| Variation | info | 
| Gene | VIPAS39 | 
| CLNDBN | not specified | 
| Reversed | 0 | 
| HGVS | NC_000014.8:g.77919702C>T | 
| CLNSRC | |
| CLNACC | RCV000171225.3, | 
