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: rs4894797
rs4894797 		3 172065756 intron variant G/A snv 0.47
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4894803
rs4894803 		3 172082466 intron variant A/G snv 0.33
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs62281815
rs62281815 		3 172252520 intron variant A/T snv 0.41
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs62283814
rs62283814 		3 172103766 intron variant C/T snv 0.18
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs6445046
rs6445046 		3 172215462 intron variant G/A;T snv
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.700 1.000 1 2018 2018
dbSNP: rs6445055
rs6445055 		0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6445055
rs6445055 		0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6445055
rs6445055 		0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.700 1.000 1 2013 2013
dbSNP: rs6763687
rs6763687 		3 172059856 intron variant A/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs6763687
rs6763687 		3 172059856 intron variant A/G;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs7652177
rs7652177 		3 172251287 missense variant C/G snv 0.54 0.61
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs9647379
rs9647379 		3 172067378 intron variant G/C snv 0.32
CUI: C0018810
Disease: heart rate
heart rate 		0.800 1.000 1 2013 2013