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.
] 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.
] 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
] 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, | 


