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rs9288410

From SNPedia

Orientationplus
Stabilizedplus
Make rs9288410(A;A)
Make rs9288410(A;G)
Make rs9288410(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position209633537
GeneMAP2
is asnp
is mentioned by
dbSNPrs9288410
ebirs9288410
HLIrs9288410
Exacrs9288410
Varsomers9288410
Maprs9288410
PheGenIrs9288410
hapmaprs9288410
1000 genomesrs9288410
hgdprs9288410
ensemblrs9288410
gopubmedrs9288410
geneviewrs9288410
scholarrs9288410
googlers9288410
pharmgkbrs9288410
gwascentralrs9288410
openSNPrs9288410
23andMers9288410
23andMe allrs9288410
SNP Nexus

SNPshotrs9288410
SNPdbers9288410
MSV3drs9288410
GWAS Ctlgrs9288410
GMAF0.2929
Max Magnitude
? (A;A) (A;G) (G;G) 28

news

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 18541031OA-icon.png] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.