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: rs6861681
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.800 1.000 2 2010 2018
dbSNP: rs17695092
rs17695092
CPEB4
1.000 0.040 5 173910850 intron variant T/G snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs72812846
rs72812846
CPEB4
5 173950633 intron variant T/A;C snv 0.23
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2017
dbSNP: rs17076724
rs17076724
CPEB4
5 173936664 intron variant G/T snv 0.43
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs17076726
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43
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: rs17076726
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs17076726
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs359466
rs359466
CPEB4
5 173888863 5 prime UTR variant C/G snv 0.11
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs56163845
rs56163845
CPEB4
1.000 0.040 5 173946945 intron variant A/G snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs6864691
rs6864691
CPEB4
5 173931151 intron variant G/A snv 0.40
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs72810983
rs72810983
CPEB4
5 173891251 intron variant A/G snv 0.23
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs72812861
rs72812861
CPEB4
0.827 0.120 5 173960506 3 prime UTR variant T/C snv 0.22
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs72812861
rs72812861
CPEB4
0.827 0.120 5 173960506 3 prime UTR variant T/C snv 0.22
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs72812861
rs72812861
CPEB4
0.827 0.120 5 173960506 3 prime UTR variant T/C snv 0.22
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs72812861
rs72812861
CPEB4
0.827 0.120 5 173960506 3 prime UTR variant T/C snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs72812861
rs72812861
CPEB4
0.827 0.120 5 173960506 3 prime UTR variant T/C snv 0.22
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs75049939
rs75049939
CPEB4
5 173907216 intron variant T/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7705502
rs7705502
CPEB4
5 173893812 intron variant G/A snv 0.22
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs7705502
rs7705502
CPEB4
5 173893812 intron variant G/A snv 0.22
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs7705507
rs7705507
CPEB4
5 173931334 intron variant C/T snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019