rs138083522
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| Make rs138083522(C;T) |
| Make rs138083522(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 10 |
| Position | 17071457 |
| Gene | CUBN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138083522 |
| dbSNP (classic) | rs138083522 |
| ClinGen | rs138083522 |
| ebi | rs138083522 |
| HLI | rs138083522 |
| Exac | rs138083522 |
| Gnomad | rs138083522 |
| Varsome | rs138083522 |
| LitVar | rs138083522 |
| Map | rs138083522 |
| PheGenI | rs138083522 |
| Biobank | rs138083522 |
| 1000 genomes | rs138083522 |
| hgdp | rs138083522 |
| ensembl | rs138083522 |
| geneview | rs138083522 |
| scholar | rs138083522 |
| rs138083522 | |
| pharmgkb | rs138083522 |
| gwascentral | rs138083522 |
| openSNP | rs138083522 |
| 23andMe | rs138083522 |
| SNPshot | rs138083522 |
| SNPdbe | rs138083522 |
| MSV3d | rs138083522 |
| GWAS Ctlg | rs138083522 |
| Max Magnitude | 0 |
CUBN gene, c.2594G>A (p.Ser865Asn)
minor allele reported as pathogenic in ClinVar but condition not specified
| ClinVar | |
|---|---|
| Risk | rs138083522(A;A) rs138083522(T;T) |
| Alt | rs138083522(A;A) rs138083522(T;T) |
| Reference | Rs138083522(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CUBN |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.17113456C>T |
| CLNSRC | |
| CLNACC | RCV000255679.1, |
