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: rs4894535
rs4894535 		1.000 0.040 3 172277815 intron variant C/A;T snv
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.800 1.000 1 2013 2013
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
dbSNP: rs7652177
rs7652177 		3 172251287 missense variant C/G snv 0.54 0.61
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs7635832
rs7635832 		3 172271486 intron variant T/G snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 3 2017 2018
dbSNP: rs12492846
rs12492846 		3 172208901 intron variant C/T snv 0.73
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2018 2018
dbSNP: rs4243400
rs4243400 		3 172253069 intron variant A/G snv 0.60
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs6445055
rs6445055 		0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2014 2017
dbSNP: rs9647379
rs9647379 		3 172067378 intron variant G/C snv 0.32
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs11718418
rs11718418 		3 172053964 intron variant A/G snv 0.55
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12493901
rs12493901 		3 172204265 intron variant G/A snv 0.37
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12493901
rs12493901 		3 172204265 intron variant G/A snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs12493901
rs12493901 		3 172204265 intron variant G/A snv 0.37
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs12897
rs12897 		1.000 0.040 3 172398112 3 prime UTR variant G/A snv 0.47
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs16856859
rs16856859 		3 172066946 intron variant A/G snv 0.48
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs16856859
rs16856859 		3 172066946 intron variant A/G snv 0.48
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs16856911
rs16856911 		3 172082708 intron variant G/C snv 5.8E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs35461662
rs35461662 		3 172056222 intron variant T/A;C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs35461662
rs35461662 		3 172056222 intron variant T/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs397778518
rs397778518 		3 172081346 intron variant -/T;TT delins 0.49
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4380442
rs4380442 		3 172212591 intron variant G/A snv 0.90
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs4535251
rs4535251 		3 172208583 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs4535251
rs4535251 		3 172208583 intron variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs4894539
rs4894539 		3 172281493 intron variant G/T snv 0.53
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4894797
rs4894797 		3 172065756 intron variant G/A snv 0.47
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
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