rs1834640
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs1834640(A;G) |
Make rs1834640(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 48099968 |
is a | snp |
is | mentioned by |
dbSNP | rs1834640 |
dbSNP (classic) | rs1834640 |
ClinGen | rs1834640 |
ebi | rs1834640 |
HLI | rs1834640 |
Exac | rs1834640 |
Gnomad | rs1834640 |
Varsome | rs1834640 |
LitVar | rs1834640 |
Map | rs1834640 |
PheGenI | rs1834640 |
Biobank | rs1834640 |
1000 genomes | rs1834640 |
hgdp | rs1834640 |
ensembl | rs1834640 |
geneview | rs1834640 |
scholar | rs1834640 |
rs1834640 | |
pharmgkb | rs1834640 |
gwascentral | rs1834640 |
openSNP | rs1834640 |
23andMe | rs1834640 |
SNPshot | rs1834640 |
SNPdbe | rs1834640 |
MSV3d | rs1834640 |
GWAS Ctlg | rs1834640 |
GMAF | 0.4927 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs1834640 |
PubMedID | [PMID 17999355] |
Condition | Skin pigmentation by reflectance spectroscopy |
Gene | SLC24A5 |
Risk Allele | G |
pValue | 1.00E-050 |
OR | 12.5 |
95% CI | 8.33-20.0 |
[PMID 21253569] Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
[PMID 23815888] Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel.