WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
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: C1720164
Disease: Central corneal thickness
Central corneal thickness
0.700 1.000 2 2016 2018
dbSNP: rs9330813
rs9330813
1.000 0.040 22 45968281 intron variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 2 2016 2019
dbSNP: rs10453441
rs10453441
1.000 0.040 22 45967859 intron variant A/G snv 0.40
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.700 1.000 1 2015 2015
dbSNP: rs9330813
rs9330813
1.000 0.040 22 45968281 intron variant G/A;C snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs9330813
rs9330813
1.000 0.040 22 45968281 intron variant G/A;C snv
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness
0.700 1.000 1 2018 2018
dbSNP: rs1475762618
rs1475762618
1.000 0.080 22 45923167 missense variant G/A snv
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1569119395
rs1569119395
0.925 0.120 22 45949926 stop gained G/A snv
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1569119395
rs1569119395
0.925 0.120 22 45949926 stop gained G/A snv
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases 0.700 0
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