WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Myopia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10453441
rs10453441 		1.000 0.040 22 45967859 intron variant A/G snv 0.40
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.020 1.000 2 2015 2018
dbSNP: rs200329677
rs200329677 		1.000 0.040 22 45973898 intron variant C/T snv 1.4E-05
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9330813
rs9330813 		1.000 0.040 22 45968281 intron variant G/A;C snv
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.010 1.000 1 2018 2018