rs17018757
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(I;I) | 0 |
Make rs17018757(-;-) |
Make rs17018757(-;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 91112088 |
Gene | LUM |
is a | snp |
is | mentioned by |
dbSNP | rs17018757 |
dbSNP (classic) | rs17018757 |
ClinGen | rs17018757 |
ebi | rs17018757 |
HLI | rs17018757 |
Exac | rs17018757 |
Gnomad | rs17018757 |
Varsome | rs17018757 |
LitVar | rs17018757 |
Map | rs17018757 |
PheGenI | rs17018757 |
Biobank | rs17018757 |
1000 genomes | rs17018757 |
hgdp | rs17018757 |
ensembl | rs17018757 |
geneview | rs17018757 |
scholar | rs17018757 |
rs17018757 | |
pharmgkb | rs17018757 |
gwascentral | rs17018757 |
openSNP | rs17018757 |
23andMe | rs17018757 |
SNPshot | rs17018757 |
SNPdbe | rs17018757 |
MSV3d | rs17018757 |
GWAS Ctlg | rs17018757 |
GMAF | 0.07989 |
Max Magnitude | 0 |
[PMID 19643966] Association of the Lumican gene functional 3' UTR polymorphism with high myopia
[PMID 21885486] Association Analysis of Polymorphisms in Lumican Gene and Systemic Lupus Erythematosus in a Taiwan Chinese Han Population