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rs3026393

From SNPedia

Orientationminus
Stabilizedminus
Make rs3026393(G;G)
Make rs3026393(G;T)
Make rs3026393(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position31790667
GenePAX6
is asnp
is mentioned by
dbSNPrs3026393
ebirs3026393
HLIrs3026393
Exacrs3026393
Varsomers3026393
Maprs3026393
PheGenIrs3026393
hapmaprs3026393
1000 genomesrs3026393
hgdprs3026393
ensemblrs3026393
gopubmedrs3026393
geneviewrs3026393
scholarrs3026393
googlers3026393
pharmgkbrs3026393
gwascentralrs3026393
openSNPrs3026393
23andMers3026393
23andMe allrs3026393
SNP Nexus

SNPshotrs3026393
SNPdbers3026393
MSV3drs3026393
GWAS Ctlgrs3026393
GMAF0.4509
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 19124844] rs3026390 and rs3026393 showed significant association with high myopia. For rs3026393, the genotype relative risk was 2.57 for (G;T) and 2.22 for (T;T) vs (G;G)


[PMID 19607881] A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient


[PMID 21589860OA-icon.png] PAX6 haplotypes are associated with high myopia in Han chinese


[PMID 19142206OA-icon.png] Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations.


[PMID 19907666OA-icon.png] AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia.


[PMID 21348901] PAX6 polymorphisms in 20 Chinese children with supernumerary teeth in the maxillary incisor area.