rs1048612
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1048612(C;C) |
| Make rs1048612(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 83783414 |
| Gene | CDH13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048612 |
| dbSNP (classic) | rs1048612 |
| ClinGen | rs1048612 |
| ebi | rs1048612 |
| HLI | rs1048612 |
| Exac | rs1048612 |
| Gnomad | rs1048612 |
| Varsome | rs1048612 |
| LitVar | rs1048612 |
| Map | rs1048612 |
| PheGenI | rs1048612 |
| Biobank | rs1048612 |
| 1000 genomes | rs1048612 |
| hgdp | rs1048612 |
| ensembl | rs1048612 |
| geneview | rs1048612 |
| scholar | rs1048612 |
| rs1048612 | |
| pharmgkb | rs1048612 |
| gwascentral | rs1048612 |
| openSNP | rs1048612 |
| 23andMe | rs1048612 |
| SNPshot | rs1048612 |
| SNPdbe | rs1048612 |
| MSV3d | rs1048612 |
| GWAS Ctlg | rs1048612 |
| GMAF | 0.1795 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24142632
] Association between CDH13 Variants and Cardiometabolic and Vascular Phenotypes in a Korean Population
| ClinVar | |
|---|---|
| Risk | rs1048612(C;C) |
| Alt | rs1048612(C;C) |
| Reference | Rs1048612(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | CDH13 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000016.9:g.83817019A>G |
| CLNSRC | |
| CLNACC | RCV000254546.1, |
