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rs2842992

From SNPedia

Orientationminus
Stabilizedminus
Make rs2842992(C;C)
Make rs2842992(C;T)
Make rs2842992(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position159650127
is asnp
is mentioned by
dbSNPrs2842992
ebirs2842992
HLIrs2842992
Exacrs2842992
Varsomers2842992
Maprs2842992
PheGenIrs2842992
hapmaprs2842992
1000 genomesrs2842992
hgdprs2842992
ensemblrs2842992
gopubmedrs2842992
geneviewrs2842992
scholarrs2842992
googlers2842992
pharmgkbrs2842992
gwascentralrs2842992
openSNPrs2842992
23andMers2842992
23andMe allrs2842992
SNP Nexus

SNPshotrs2842992
SNPdbers2842992
MSV3drs2842992
GWAS Ctlgrs2842992
GMAF0.3338
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22705344OA-icon.png]
Trait
Title Heritability and Genome-Wide Association Study to Assess Genetic Differences between Advanced Age-Related Macular Degeneration Subtypes.
Risk Allele
P-val 3E-7
Odds Ratio 1.4300 None