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, |