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rs284489

From SNPedia

Orientationplus
Stabilizedplus
Make rs284489(A;A)
Make rs284489(A;G)
Make rs284489(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position104945792
is asnp
is mentioned by
dbSNPrs284489
ebirs284489
HLIrs284489
Exacrs284489
Varsomers284489
Maprs284489
PheGenIrs284489
hapmaprs284489
1000 genomesrs284489
hgdprs284489
ensemblrs284489
gopubmedrs284489
geneviewrs284489
scholarrs284489
googlers284489
pharmgkbrs284489
gwascentralrs284489
openSNPrs284489
23andMers284489
23andMe allrs284489
SNP Nexus

SNPshotrs284489
SNPdbers284489
MSV3drs284489
GWAS Ctlgrs284489
GMAF0.4435
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22570617OA-icon.png]
Trait
Title Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
Risk Allele
P-val 9E-10
Odds Ratio 1.6100 None