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: rs848512
rs848512 		1.000 0.080 2 36448387 intron variant A/G snv 0.75
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 1 2013 2013
dbSNP: rs848602
rs848602 		2 36551229 intron variant G/A snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2019 2019
dbSNP: rs145029810
rs145029810 		2 36355997 5 prime UTR variant G/A snv 2.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17018786
rs17018786 		2 36435390 intron variant G/C snv 1.9E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs181698387
rs181698387 		2 36355677 upstream gene variant T/A;C;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2216099
rs2216099 		2 36416990 intron variant G/A snv 0.47
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs3755206
rs3755206 		2 36456285 intron variant T/G snv 2.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs3821169
rs3821169 		2 36356318 missense variant G/T snv 3.6E-02 1.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6708545
rs6708545 		2 36354324 upstream gene variant G/A snv 0.65
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs711245
rs711245 		2 36541732 intron variant G/A snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs7562790
rs7562790 		2 36446412 intron variant T/G snv 0.48
CUI: C0018803
Disease: Heart Function Tests
Heart Function Tests 		0.700 1.000 1 2010 2010
dbSNP: rs7562790
rs7562790 		2 36446412 intron variant T/G snv 0.48
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs113372122
rs113372122 		0.882 0.040 2 36479557 missense variant A/C snv 1.7E-03 1.7E-03
CUI: C0033999
Disease: Pterygium
Pterygium 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs113372122
rs113372122 		0.882 0.040 2 36479557 missense variant A/C snv 1.7E-03 1.7E-03
CUI: C4520843
Disease: Pterygium of eye
Pterygium of eye 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs113372122
rs113372122 		0.882 0.040 2 36479557 missense variant A/C snv 1.7E-03 1.7E-03
CUI: C1867441
Disease: Pterygium Of Conjunctiva And Cornea
Pterygium Of Conjunctiva And Cornea 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs711254
rs711254 		1.000 0.080 2 36453705 intron variant A/G snv 0.76
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2013 2013