FOXO3, forkhead box O3, 2309

N. diseases: 381; N. variants: 30
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: rs9400239
rs9400239 		1.000 6 108656460 5 prime UTR variant T/C snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs3800229
rs3800229 		1.000 0.040 6 108675760 intron variant G/T snv 0.54
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2017
dbSNP: rs12206094
rs12206094 		6 108584997 intron variant C/T snv 0.31
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12206094
rs12206094 		6 108584997 intron variant C/T snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1536057
rs1536057 		1.000 0.040 6 108564420 intron variant C/T snv 0.30
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17069665
rs17069665 		0.882 0.120 6 108620265 intron variant A/C;G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2020 2020
dbSNP: rs2253310
rs2253310 		6 108567390 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2764261
rs2764261 		6 108606639 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2764261
rs2764261 		6 108606639 intron variant A/G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2802288
rs2802288 		6 108575012 intron variant A/G snv 0.50
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs3800229
rs3800229 		1.000 0.040 6 108675760 intron variant G/T snv 0.54
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3800229
rs3800229 		1.000 0.040 6 108675760 intron variant G/T snv 0.54
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs3800230
rs3800230 		6 108676925 intron variant T/G snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3813498
rs3813498 		6 108622962 intron variant C/T snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs9398171
rs9398171 		1.000 0.040 6 108662324 intron variant C/T snv 0.55
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs9400239
rs9400239 		1.000 6 108656460 5 prime UTR variant T/C snv 0.55
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs9400239
rs9400239 		1.000 6 108656460 5 prime UTR variant T/C snv 0.55
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2015 2015
dbSNP: rs9400241
rs9400241 		0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2020 2020
dbSNP: rs9480865
rs9480865 		6 108595370 intron variant T/C snv 0.18
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs9480866
rs9480866 		6 108641439 intron variant C/T snv 0.19
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9486913
rs9486913 		6 108639637 intron variant C/G snv 0.20
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4946935
rs4946935 		1.000 0.040 6 108679539 intron variant A/G snv 0.54
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs2022464
rs2022464 		6 108624167 intron variant A/C;T snv 0.56
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2490272
rs2490272 		6 108574183 intron variant C/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017