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rs112000638

From SNPedia

Orientationplus
Stabilizedplus
Make rs112000638(C;C)
Make rs112000638(C;T)
Make rs112000638(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position131359434
is asnp
is mentioned by
dbSNPrs112000638
ebirs112000638
HLIrs112000638
Exacrs112000638
Varsomers112000638
Maprs112000638
PheGenIrs112000638
hapmaprs112000638
1000 genomesrs112000638
hgdprs112000638
ensemblrs112000638
gopubmedrs112000638
geneviewrs112000638
scholarrs112000638
googlers112000638
pharmgkbrs112000638
gwascentralrs112000638
openSNPrs112000638
23andMers112000638
23andMe allrs112000638
SNP Nexus

SNPshotrs112000638
SNPdbers112000638
MSV3drs112000638
GWAS Ctlgrs112000638
GMAF0.005969
Max Magnitude

[PMID 23534868] CFH (rs1410996), HTRA1 (rs112000638) and ARMS2 (rs10490923) Gene Polymorphisms are Associated with AMD Risk in Spanish Patients