rs11218544
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11218544(G;G) |
Make rs11218544(G;T) |
Make rs11218544(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 122168344 |
Gene | MIR100HG |
is a | snp |
is | mentioned by |
dbSNP | rs11218544 |
dbSNP (classic) | rs11218544 |
ClinGen | rs11218544 |
ebi | rs11218544 |
HLI | rs11218544 |
Exac | rs11218544 |
Gnomad | rs11218544 |
Varsome | rs11218544 |
LitVar | rs11218544 |
Map | rs11218544 |
PheGenI | rs11218544 |
Biobank | rs11218544 |
1000 genomes | rs11218544 |
hgdp | rs11218544 |
ensembl | rs11218544 |
geneview | rs11218544 |
scholar | rs11218544 |
rs11218544 | |
pharmgkb | rs11218544 |
gwascentral | rs11218544 |
openSNP | rs11218544 |
23andMe | rs11218544 |
SNPshot | rs11218544 |
SNPdbe | rs11218544 |
MSV3d | rs11218544 |
GWAS Ctlg | rs11218544 |
GMAF | 0.2002 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
Despite two previous GWAS studies associating this SNP with high myopia in Japanese populations, no association was seen in a Chinese population studied.[PMID 22194655]
[PMID 19779542] A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.