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: rs8006385
rs8006385
ITPK1
14 93034681 intron variant A/G snv 0.13
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs7156335
rs7156335
ITPK1
14 92939887 3 prime UTR variant T/C snv 9.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2019 2019
dbSNP: rs2180369
rs2180369
ITPK1
0.925 0.040 14 93050120 intron variant T/C snv 0.13
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs2180369
rs2180369
ITPK1
0.925 0.040 14 93050120 intron variant T/C snv 0.13
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2281513
rs2281513
ITPK1
1.000 0.040 14 92937521 3 prime UTR variant C/G snv 5.1E-03
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs35584079
rs35584079
ITPK1
1.000 0.040 14 93045296 intron variant G/A snv 0.24
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs36084521
rs36084521
ITPK1
14 93050053 intron variant T/G snv 0.13
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs72706424
rs72706424
ITPK1
14 93056240 intron variant G/A;T snv 4.3E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019