rs7854658
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs7854658(A;A) |
Make rs7854658(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 126652659 |
Gene | LMX1B |
is a | snp |
is | mentioned by |
dbSNP | rs7854658 |
dbSNP (classic) | rs7854658 |
ClinGen | rs7854658 |
ebi | rs7854658 |
HLI | rs7854658 |
Exac | rs7854658 |
Gnomad | rs7854658 |
Varsome | rs7854658 |
LitVar | rs7854658 |
Map | rs7854658 |
PheGenI | rs7854658 |
Biobank | rs7854658 |
1000 genomes | rs7854658 |
hgdp | rs7854658 |
ensembl | rs7854658 |
geneview | rs7854658 |
scholar | rs7854658 |
rs7854658 | |
pharmgkb | rs7854658 |
gwascentral | rs7854658 |
openSNP | rs7854658 |
23andMe | rs7854658 |
SNPshot | rs7854658 |
SNPdbe | rs7854658 |
MSV3d | rs7854658 |
GWAS Ctlg | rs7854658 |
GMAF | 0.1919 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18952915] Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes