rs154659
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs154659(C;C) |
Make rs154659(C;T) |
Make rs154659(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 89600929 |
is a | snp |
is | mentioned by |
dbSNP | rs154659 |
dbSNP (classic) | rs154659 |
ClinGen | rs154659 |
ebi | rs154659 |
HLI | rs154659 |
Exac | rs154659 |
Gnomad | rs154659 |
Varsome | rs154659 |
LitVar | rs154659 |
Map | rs154659 |
PheGenI | rs154659 |
Biobank | rs154659 |
1000 genomes | rs154659 |
hgdp | rs154659 |
ensembl | rs154659 |
geneview | rs154659 |
scholar | rs154659 |
rs154659 | |
pharmgkb | rs154659 |
gwascentral | rs154659 |
openSNP | rs154659 |
23andMe | rs154659 |
SNPshot | rs154659 |
SNPdbe | rs154659 |
MSV3d | rs154659 |
GWAS Ctlg | rs154659 |
GMAF | 0.36 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19340012] |
Trait | Tanning |
Title | Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry |
Risk Allele | C |
P-val | 7E-8 |
Odds Ratio |
[PMID 18076761] In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.
[PMID 19366436] Whole genome amplification and real-time PCR in forensic casework.
[PMID 20585627] Web-based, participant-driven studies yield novel genetic associations for common traits.