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: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2014 2014
dbSNP: rs1800564
rs1800564
LEP
1.000 0.080 7 128254587 missense variant G/A;T snv 1.5E-04; 4.0E-06
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2012 2012
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: 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: rs13228377
rs13228377
LEP
1.000 0.080 7 128239891 upstream gene variant A/C;G snv
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2018 2018
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: rs200487063
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05
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: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast 		0.010 1.000 1 2015 2015
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		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: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma 		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: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2008 2008
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: 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: rs200487063
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		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: 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: rs200487063
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05
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: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015
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: rs1554394014
rs1554394014
LEP
1.000 7 128254720 missense variant T/C snv
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.700 0
dbSNP: rs724159998
rs724159998
LEP
0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.700 0
dbSNP: rs724159998
rs724159998
LEP
0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06
CUI: C4016279
Disease: LEPTIN DYSFUNCTION
LEPTIN DYSFUNCTION 		0.700 0
dbSNP: rs2167270
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs2071045
rs2071045
LEP
0.925 0.120 7 128252927 intron variant T/C snv 0.18
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		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: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2014 2014