rs2733832
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs2733832(C;T) |
| Make rs2733832(T;T) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 9 |
| Position | 12704725 |
| Gene | LURAP1L-AS1, TYRP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2733832 |
| dbSNP (classic) | rs2733832 |
| ClinGen | rs2733832 |
| ebi | rs2733832 |
| HLI | rs2733832 |
| Exac | rs2733832 |
| Gnomad | rs2733832 |
| Varsome | rs2733832 |
| LitVar | rs2733832 |
| Map | rs2733832 |
| PheGenI | rs2733832 |
| Biobank | rs2733832 |
| 1000 genomes | rs2733832 |
| hgdp | rs2733832 |
| ensembl | rs2733832 |
| geneview | rs2733832 |
| scholar | rs2733832 |
| rs2733832 | |
| pharmgkb | rs2733832 |
| gwascentral | rs2733832 |
| openSNP | rs2733832 |
| 23andMe | rs2733832 |
| SNPshot | rs2733832 |
| SNPdbe | rs2733832 |
| MSV3d | rs2733832 |
| GWAS Ctlg | rs2733832 |
| GMAF | 0.2792 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Influences appearance gnxp
[PMID 17999355
] A genomewide association study of skin pigmentation in a South Asian population.
[PMID 18312627
] Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans.
[PMID 25837821
] Inherited genetic variants associated with occurrence of multiple primary melanoma
| ClinVar | |
|---|---|
| Risk | rs2733832(G;G) rs2733832(T;T) |
| Alt | rs2733832(G;G) rs2733832(T;T) |
| Reference | Rs2733832(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | TYRP1 LURAP1L-AS1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000009.11:g.12704725C>T |
| CLNSRC | |
| CLNACC | RCV000251189.1, |
