Source: ALL

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: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 3 2012 2019
dbSNP: rs4987856
rs4987856
0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 2 2013 2016
dbSNP: rs4987852
rs4987852
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2013
dbSNP: rs4987855
rs4987855
0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2013
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 5 2016 2019
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs4940576
rs4940576
0.925 0.040 18 63181406 intron variant T/A;C snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 2 2015 2017
dbSNP: rs4940576
rs4940576
0.925 0.040 18 63181406 intron variant T/A;C snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 2 2015 2017
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement
0.700 1.000 1 2016 2016
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs17758695
rs17758695
18 63253621 intron variant C/T snv 2.1E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs187971642
rs187971642
18 63213468 intron variant T/C snv 4.1E-03
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4987852
rs4987852
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2013 2013
dbSNP: rs4987855
rs4987855
0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2013 2013