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rs10801575

From SNPedia

Orientationplus
Stabilizedplus
Make rs10801575(C;C)
Make rs10801575(C;T)
Make rs10801575(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196883651
GeneLOC100289145
is asnp
is mentioned by
dbSNPrs10801575
ebirs10801575
HLIrs10801575
Exacrs10801575
Varsomers10801575
Maprs10801575
PheGenIrs10801575
hapmaprs10801575
1000 genomesrs10801575
hgdprs10801575
ensemblrs10801575
gopubmedrs10801575
geneviewrs10801575
scholarrs10801575
googlers10801575
pharmgkbrs10801575
gwascentralrs10801575
openSNPrs10801575
23andMers10801575
23andMe allrs10801575
SNP Nexus

SNPshotrs10801575
SNPdbers10801575
MSV3drs10801575
GWAS Ctlgrs10801575
GMAF0.376
Max Magnitude
? (C;C) (C;T) (T;T) 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.