rs370356566
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs370356566(A;A) |
| Make rs370356566(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 157471733 |
| Gene | NIPAL4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs370356566 |
| dbSNP (classic) | rs370356566 |
| ClinGen | rs370356566 |
| ebi | rs370356566 |
| HLI | rs370356566 |
| Exac | rs370356566 |
| Gnomad | rs370356566 |
| Varsome | rs370356566 |
| LitVar | rs370356566 |
| Map | rs370356566 |
| PheGenI | rs370356566 |
| Biobank | rs370356566 |
| 1000 genomes | rs370356566 |
| hgdp | rs370356566 |
| ensembl | rs370356566 |
| geneview | rs370356566 |
| scholar | rs370356566 |
| rs370356566 | |
| pharmgkb | rs370356566 |
| gwascentral | rs370356566 |
| openSNP | rs370356566 |
| 23andMe | rs370356566 |
| SNPshot | rs370356566 |
| SNPdbe | rs370356566 |
| MSV3d | rs370356566 |
| GWAS Ctlg | rs370356566 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs370356566(A;A) |
| Alt | rs370356566(A;A) |
| Reference | Rs370356566(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ADAM19 NIPAL4 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.156898741G>A |
| CLNSRC | |
| CLNACC | RCV000414650.1, |
