rs1006615
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1006615(C;T) |
| Make rs1006615(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 130433393 |
| Gene | HMCN2, LOC107987134 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1006615 |
| dbSNP (classic) | rs1006615 |
| ClinGen | rs1006615 |
| ebi | rs1006615 |
| HLI | rs1006615 |
| Exac | rs1006615 |
| Gnomad | rs1006615 |
| Varsome | rs1006615 |
| LitVar | rs1006615 |
| Map | rs1006615 |
| PheGenI | rs1006615 |
| Biobank | rs1006615 |
| 1000 genomes | rs1006615 |
| hgdp | rs1006615 |
| ensembl | rs1006615 |
| geneview | rs1006615 |
| scholar | rs1006615 |
| rs1006615 | |
| pharmgkb | rs1006615 |
| gwascentral | rs1006615 |
| openSNP | rs1006615 |
| 23andMe | rs1006615 |
| SNPshot | rs1006615 |
| SNPdbe | rs1006615 |
| MSV3d | rs1006615 |
| GWAS Ctlg | rs1006615 |
| GMAF | 0.3517 |
| Max Magnitude | 0 |
[PMID 18936756] rs1006615 is associated with increased risk for schizophrenia in German and Scandinavian samples
| ClinVar | |
|---|---|
| Risk | rs1006615(A;A) rs1006615(T;T) |
| Alt | rs1006615(A;A) rs1006615(T;T) |
| Reference | Rs1006615(C;C) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | HMCN2 |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000009.12:g.130433393C>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000068558.1, |
