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: rs978332
rs978332
DLEU1 ; DLEU7
13 50562603 intron variant C/T snv 0.69
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs963740
rs963740
DLEU1 ; DLEU7 ; DLEU1-AS1
1.000 0.080 13 50521959 intron variant A/T snv 0.28
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs963740
rs963740
DLEU1 ; DLEU7 ; DLEU1-AS1
1.000 0.080 13 50521959 intron variant A/T snv 0.28
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs9596300
rs9596300
DLEU1
13 50507855 intron variant A/C;G;T snv
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
dbSNP: rs9596270
rs9596270
DLEU1
1.000 0.080 13 50268304 intron variant T/C snv 6.1E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs9591325
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs9591325
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2015 2015
dbSNP: rs9591325
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs9591325
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs9591325
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs9562955
rs9562955
DLEU1
1.000 0.040 13 50237019 intron variant G/T snv 6.4E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs9535495
rs9535495
DLEU1 ; DLEU7 ; DLEU7-AS1
13 50814824 intron variant C/T snv 0.49
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs806352
rs806352
DLEU1
13 50289783 intron variant T/G snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs806349
rs806349
DLEU1
1.000 0.080 13 50285854 intron variant C/T snv 0.41
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs806321
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 2 2011 2019
dbSNP: rs806321
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2019 2019
dbSNP: rs806321
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2019 2019
dbSNP: rs806321
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		0.700 1.000 1 2019 2019
dbSNP: rs806293
rs806293
DLEU1
13 50238846 intron variant T/A snv 0.47
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs806293
rs806293
DLEU1
13 50238846 intron variant T/A snv 0.47
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2018 2018
dbSNP: rs797487
rs797487
DLEU1 ; DLEU7
0.925 0.040 13 50650173 intron variant T/G snv 0.56
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs797487
rs797487
DLEU1 ; DLEU7
0.925 0.040 13 50650173 intron variant T/G snv 0.56
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs797486
rs797486
DLEU1 ; DLEU7
13 50647482 intron variant C/A snv 0.85
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs797486
rs797486
DLEU1 ; DLEU7
13 50647482 intron variant C/A snv 0.85
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2017 2017
dbSNP: rs780360029
rs780360029
DLEU1 ; DLEU7 ; DLEU7-AS1
13 50810602 intron variant C/T snv 3.6E-04
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2018 2018