VEGFC, vascular endothelial growth factor C, 7424

N. diseases: 291; N. variants: 12
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2333496
rs2333496
4 176688455 intron variant C/T snv 0.53
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2018 2018
dbSNP: rs41278571
rs41278571
4 176729712 missense variant C/A;T snv 1.1E-02 1.1E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs12646659
rs12646659
0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs12646659
rs12646659
0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs12646659
rs12646659
0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs1485766
rs1485766
0.882 0.120 4 176689730 intron variant T/A;G snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1485766
rs1485766
0.882 0.120 4 176689730 intron variant T/A;G snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1485766
rs1485766
0.882 0.120 4 176689730 intron variant T/A;G snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs17697305
rs17697305
4 176685497 intron variant T/C snv 2.4E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs17697305
rs17697305
4 176685497 intron variant T/C snv 2.4E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs17697419
rs17697419
1.000 0.080 4 176687012 intron variant G/A snv 8.5E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17697419
rs17697419
1.000 0.080 4 176687012 intron variant G/A snv 8.5E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17697515
rs17697515
1.000 0.080 4 176689270 intron variant C/T snv 5.1E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17697515
rs17697515
1.000 0.080 4 176689270 intron variant C/T snv 5.1E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2333526
rs2333526
1.000 0.080 4 176782151 intron variant T/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2333526
rs2333526
1.000 0.080 4 176782151 intron variant T/A;C snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3775194
rs3775194
1.000 0.080 4 176702723 intron variant C/G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs4604006
rs4604006
0.882 0.080 4 176687621 intron variant T/C snv 0.58
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs4604006
rs4604006
0.882 0.080 4 176687621 intron variant T/C snv 0.58
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs4604006
rs4604006
0.882 0.080 4 176687621 intron variant T/C snv 0.58
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs587777567
rs587777567
1.000 0.040 4 176711575 stop gained G/A snv
CUI: C1704423
Disease: Milroy Disease
Milroy Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7664413
rs7664413
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs7664413
rs7664413
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7664413
rs7664413
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7664413
rs7664413
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2013 2013