Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6684205
rs6684205
TGFB2
1 218436360 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs1890995
rs1890995
TGFB2
1 218431336 intron variant G/A snv 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs991967
rs991967
TGFB2 ; TGFB2-OT1
1 218442109 3 prime UTR variant A/C snv 0.37
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs10482792
rs10482792
TGFB2
1 218432119 intron variant G/A snv 0.33
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs10482792
rs10482792
TGFB2
1 218432119 intron variant G/A snv 0.33
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs10482795
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10482795
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10482796
rs10482796
TGFB2
1 218432293 intron variant T/C snv 0.22
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs10482796
rs10482796
TGFB2
1 218432293 intron variant T/C snv 0.22
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs10746379
rs10746379
TGFB2
1 218402545 intron variant A/G snv 0.20
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs10863398
rs10863398
TGFB2
1 218414937 intron variant G/A;C snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs10863398
rs10863398
TGFB2
1 218414937 intron variant G/A;C snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs11118102
rs11118102
TGFB2
1 218398662 intron variant G/A snv 0.17
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs113711540
rs113711540
TGFB2 ; TGFB2-AS1
1 218346586 5 prime UTR variant -/CAA delins
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs12048049
rs12048049
TGFB2
1 218423955 intron variant C/G snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs12048049
rs12048049
TGFB2
1 218423955 intron variant C/G snv 0.37
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs12048582
rs12048582
TGFB2
1 218419695 intron variant C/G;T snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs12048582
rs12048582
TGFB2
1 218419695 intron variant C/G;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs12088448
rs12088448
TGFB2
1 218372828 intron variant A/C snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1317681
rs1317681
TGFB2
1 218401860 intron variant G/A snv 0.19
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs1342586
rs1342586
TGFB2
1 218424517 intron variant C/T snv 0.22
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs1342586
rs1342586
TGFB2
1 218424517 intron variant C/T snv 0.22
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs1417488
rs1417488
TGFB2
1 218350388 intron variant C/T snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17047703
rs17047703
TGFB2
1 218352246 intron variant C/A snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs17047804
rs17047804
TGFB2
1 218409436 intron variant T/C snv 0.18
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015