rs3759222
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3759222(A;A) |
Make rs3759222(A;C) |
Make rs3759222(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 91113176 |
Gene | LUM |
is a | snp |
is | mentioned by |
dbSNP | rs3759222 |
dbSNP (classic) | rs3759222 |
ClinGen | rs3759222 |
ebi | rs3759222 |
HLI | rs3759222 |
Exac | rs3759222 |
Gnomad | rs3759222 |
Varsome | rs3759222 |
LitVar | rs3759222 |
Map | rs3759222 |
PheGenI | rs3759222 |
Biobank | rs3759222 |
1000 genomes | rs3759222 |
hgdp | rs3759222 |
ensembl | rs3759222 |
geneview | rs3759222 |
scholar | rs3759222 |
rs3759222 | |
pharmgkb | rs3759222 |
gwascentral | rs3759222 |
openSNP | rs3759222 |
23andMe | rs3759222 |
SNPshot | rs3759222 |
SNPdbe | rs3759222 |
MSV3d | rs3759222 |
GWAS Ctlg | rs3759222 |
GMAF | 0.3104 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23145541] Absence of an association between lumican promoter variants and high myopia in the Korean population