rs11012732
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(A;G) | 1.4 | 1.4x increased risk for meningioma |
(G;G) | 2 | 2x increased risk for meningioma |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 21541175 |
Gene | MLLT10 |
is a | snp |
is | mentioned by |
dbSNP | rs11012732 |
dbSNP (classic) | rs11012732 |
ClinGen | rs11012732 |
ebi | rs11012732 |
HLI | rs11012732 |
Exac | rs11012732 |
Gnomad | rs11012732 |
Varsome | rs11012732 |
LitVar | rs11012732 |
Map | rs11012732 |
PheGenI | rs11012732 |
Biobank | rs11012732 |
1000 genomes | rs11012732 |
hgdp | rs11012732 |
ensembl | rs11012732 |
geneview | rs11012732 |
scholar | rs11012732 |
rs11012732 | |
pharmgkb | rs11012732 |
gwascentral | rs11012732 |
openSNP | rs11012732 |
23andMe | rs11012732 |
SNPshot | rs11012732 |
SNPdbe | rs11012732 |
MSV3d | rs11012732 |
GWAS Ctlg | rs11012732 |
GMAF | 0.2259 |
Max Magnitude | 2 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs11012732 is a SNP in the MLLT10 gene on ch 10p12.31.
A study of ~1,600 patients with meningioma, all of European ancestry, concluded that increased risk for the disease was associated with rs11012732(G) alleles. The odds ratio was 1.46 (p = 1.9 x 10e-14). A nearby SNP, rs12770228, was also linked to meningioma risk.[PMID 21804547]