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rs955943

From SNPedia

Orientationminus
Stabilizedminus
Make rs955943(A;A)
Make rs955943(A;G)
Make rs955943(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position16512785
GeneLDB2
is asnp
is mentioned by
dbSNPrs955943
ebirs955943
HLIrs955943
Exacrs955943
Varsomers955943
Maprs955943
PheGenIrs955943
hapmaprs955943
1000 genomesrs955943
hgdprs955943
ensemblrs955943
gopubmedrs955943
geneviewrs955943
scholarrs955943
googlers955943
pharmgkbrs955943
gwascentralrs955943
openSNPrs955943
23andMers955943
23andMe allrs955943
SNP Nexus

SNPshotrs955943
SNPdbers955943
MSV3drs955943
GWAS Ctlgrs955943
GMAF0.0932
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23585552]
Trait Rhegmatogenous retinal detachment
Title Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
Risk Allele A
P-val 5E-6
Odds Ratio 1.41 [1.21-1.64]