Source: BEFREE

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: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0028754
Disease: Obesity
Obesity
0.100 1.000 10 2001 2018
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 1.000 4 2011 2017
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
Diabetes Mellitus, Non-Insulin-Dependent
0.040 0.750 4 2005 2019
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 1.000 4 2011 2017
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 1.000 2 2012 2019
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.020 1.000 2 2013 2018
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.020 1.000 2 2010 2015
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 0.500 2 2003 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
0.020 1.000 2 2001 2005
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 0.500 2 2003 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.020 1.000 2 2010 2015
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0023895
Disease: Liver diseases
Liver diseases
0.010 1.000 1 2013 2013
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 < 0.001 1 2019 2019
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0080178
Disease: Spina Bifida
Spina Bifida
0.010 1.000 1 2011 2011
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2017 2017
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
Childhood Acute Lymphoblastic Leukemia
0.010 < 0.001 1 2011 2011
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 1.000 1 2013 2013
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2
0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 < 0.001 1 2019 2019