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rs3759223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0
Make rs3759223(C;C)
Make rs3759223(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position91113006
GeneLUM
is asnp
is mentioned by
dbSNPrs3759223
dbSNP (classic)rs3759223
ClinGenrs3759223
ebirs3759223
HLIrs3759223
Exacrs3759223
Gnomadrs3759223
Varsomers3759223
LitVarrs3759223
Maprs3759223
PheGenIrs3759223
Biobankrs3759223
1000 genomesrs3759223
hgdprs3759223
ensemblrs3759223
geneviewrs3759223
scholarrs3759223
googlers3759223
pharmgkbrs3759223
gwascentralrs3759223
openSNPrs3759223
23andMers3759223
SNPshotrs3759223
SNPdbers3759223
MSV3drs3759223
GWAS Ctlgrs3759223
GMAF0.08035
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19643966] Association of the Lumican gene functional 3' UTR polymorphism with high myopia

[PMID 16902402] The association of single nucleotide polymorphisms in the 5'-regulatory region of the lumican gene with susceptibility to high myopia in Taiwan.

[PMID 19060265] High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes.

[PMID 19616852] The association of haplotype at the lumican gene with high myopia susceptibility in Taiwanese patients.

[PMID 20339468OA-icon.png] Association of lumican gene with susceptibility to pathological myopia in the northern han ethnic chinese.


[PMID 23145541] Absence of an association between lumican promoter variants and high myopia in the Korean population


[PMID 24061151] Association of Lumican Gene Polymorphism With High Myopia: A Meta-Analysis


[PMID 24927138] Lack of Association Between LUM rs3759223 Polymorphism and High Myopia