rs149969786
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs149969786(A;G) |
| Make rs149969786(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 15 |
| Position | 42410949 |
| Gene | CAPN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149969786 |
| dbSNP (classic) | rs149969786 |
| ClinGen | rs149969786 |
| ebi | rs149969786 |
| HLI | rs149969786 |
| Exac | rs149969786 |
| Gnomad | rs149969786 |
| Varsome | rs149969786 |
| LitVar | rs149969786 |
| Map | rs149969786 |
| PheGenI | rs149969786 |
| Biobank | rs149969786 |
| 1000 genomes | rs149969786 |
| hgdp | rs149969786 |
| ensembl | rs149969786 |
| geneview | rs149969786 |
| scholar | rs149969786 |
| rs149969786 | |
| pharmgkb | rs149969786 |
| gwascentral | rs149969786 |
| openSNP | rs149969786 |
| 23andMe | rs149969786 |
| SNPshot | rs149969786 |
| SNPdbe | rs149969786 |
| MSV3d | rs149969786 |
| GWAS Ctlg | rs149969786 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149969786(G;G) |
| Alt | rs149969786(G;G) |
| Reference | Rs149969786(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CAPN3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.42703147A>G |
| CLNSRC | |
| CLNACC | RCV000171232.1, |
