rs9288410
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9288410(A;A) |
Make rs9288410(A;G) |
Make rs9288410(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 209633537 |
Gene | MAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs9288410 |
dbSNP (classic) | rs9288410 |
ClinGen | rs9288410 |
ebi | rs9288410 |
HLI | rs9288410 |
Exac | rs9288410 |
Gnomad | rs9288410 |
Varsome | rs9288410 |
LitVar | rs9288410 |
Map | rs9288410 |
PheGenI | rs9288410 |
Biobank | rs9288410 |
1000 genomes | rs9288410 |
hgdp | rs9288410 |
ensembl | rs9288410 |
geneview | rs9288410 |
scholar | rs9288410 |
rs9288410 | |
pharmgkb | rs9288410 |
gwascentral | rs9288410 |
openSNP | rs9288410 |
23andMe | rs9288410 |
SNPshot | rs9288410 |
SNPdbe | rs9288410 |
MSV3d | rs9288410 |
GWAS Ctlg | rs9288410 |
GMAF | 0.2929 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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rs572515 was the most significantly associated with AMD risk (P <10-6).
rs9288410 and rs2014307 (PLEKHA1/HTRA1) on 10q26 were significantly associated with AMD status (P= .03 and P <10-6 respectively). After controlling for smoking history, gender and age, the most significant gene-gene interaction appears to be between rs10801575 (CFH) and rs2014307 (PLEKHA1/HTRA1) (P <10-11).
[PMID 18541031] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.