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rs7854658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7854658(A;A)
Make rs7854658(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position126652659
GeneLMX1B
is asnp
is mentioned by
dbSNPrs7854658
ebirs7854658
HLIrs7854658
Exacrs7854658
Varsomers7854658
Maprs7854658
PheGenIrs7854658
hapmaprs7854658
1000 genomesrs7854658
hgdprs7854658
ensemblrs7854658
gopubmedrs7854658
geneviewrs7854658
scholarrs7854658
googlers7854658
pharmgkbrs7854658
gwascentralrs7854658
openSNPrs7854658
23andMers7854658
23andMe allrs7854658
SNP Nexus

SNPshotrs7854658
SNPdbers7854658
MSV3drs7854658
GWAS Ctlgrs7854658
GMAF0.1919
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 18952915] Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes