WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10453441
rs10453441
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0027092
Disease:
Myopia
0.020 GeneticVariation BEFREE WNT7B SNPs located in the same genomic region that includes rs9330813 have previously been associated with CCT in Latinos but with other ocular quantitative traits related to myopia (corneal curvature and axial length) in a Japanese population (rs10453441 and rs200329677). 29847655 2018
dbSNP: rs10453441
rs10453441
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0027092
Disease:
Myopia
0.020 GeneticVariation BEFREE We identify WNT7B as a novel susceptibility gene for axial length (rs10453441, Pmeta=3.9 × 10(-13)) and corneal curvature (Pmeta=2.9 × 10(-40)) and confirm the previously reported association between GJD2 and myopia. 25823570 2015
dbSNP: rs200329677
rs200329677
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0027092
Disease:
Myopia
0.010 GeneticVariation BEFREE WNT7B SNPs located in the same genomic region that includes rs9330813 have previously been associated with CCT in Latinos but with other ocular quantitative traits related to myopia (corneal curvature and axial length) in a Japanese population (rs10453441 and rs200329677). 29847655 2018
dbSNP: rs9330813
rs9330813
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0027092
Disease:
Myopia
0.010 GeneticVariation BEFREE WNT7B SNPs located in the same genomic region that includes rs9330813 have previously been associated with CCT in Latinos but with other ocular quantitative traits related to myopia (corneal curvature and axial length) in a Japanese population (rs10453441 and rs200329677). 29847655 2018