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: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2014 2014
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2017 2017
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 < 0.001 1 2011 2011
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 < 0.001 1 2011 2011
dbSNP: rs34104384
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015
dbSNP: rs34104384
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03
CUI: C0242787
Disease: Malignant neoplasm of male breast
Malignant neoplasm of male breast 		0.010 1.000 1 2015 2015
dbSNP: rs34104384
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03
CUI: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast 		0.010 1.000 1 2015 2015
dbSNP: rs34104384
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2015 2015
dbSNP: rs34104384
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2015 2015
dbSNP: rs3828942
rs3828942
LEP
7 128254252 intron variant G/A snv 0.37
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2019 2019
dbSNP: rs4731426
rs4731426
LEP
1.000 0.080 7 128242017 intron variant G/A;C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs724159998
rs724159998
LEP
0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2015 2015
dbSNP: rs760165439
rs760165439
LEP
1.000 0.080 7 128252062 missense variant A/G snv 8.0E-06
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018
dbSNP: rs104894023
rs104894023
LEP
1.000 7 128254572 missense variant C/T snv
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 1.000 2 1998 2015
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2014 2018
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2014 2019
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2014 2019
dbSNP: rs28954113
rs28954113
LEP
1.000 0.080 7 128254568 missense variant C/A;T snv 2.0E-05; 1.8E-03
CUI: C0028754
Disease: Obesity
Obesity 		0.030 1.000 3 2010 2016