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: rs1178552124
rs1178552124
1.000 0.040 14 103703253 synonymous variant G/A snv
CUI: C0029172
Disease: Oral Submucous Fibrosis
Oral Submucous Fibrosis
0.010 1.000 1 2012 2012
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 < 0.001 1 2013 2013
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 < 0.001 1 2014 2014
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 < 0.001 1 2013 2013
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.010 < 0.001 1 2014 2014
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 < 0.001 1 2013 2013
dbSNP: rs1297812518
rs1297812518
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs1360602468
rs1360602468
0.925 0.080 14 103698904 missense variant G/C;T snv
Squamous cell carcinoma of the head and neck
0.010 1.000 1 2011 2011
dbSNP: rs1360602468
rs1360602468
0.925 0.080 14 103698904 missense variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs149642280
rs149642280
14 103699501 missense variant C/T snv 1.0E-04; 4.0E-06 3.5E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 < 0.001 2 2003 2006
dbSNP: rs149642280
rs149642280
14 103699501 missense variant C/T snv 1.0E-04; 4.0E-06 3.5E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 < 0.001 2 2003 2006
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.060 0.667 6 2011 2017
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.060 0.667 6 2011 2017
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 0.500 2 2015 2016
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.020 1.000 2 2013 2014
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 0.500 2 2015 2016
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
Malignant neoplasm of urinary bladder
0.010 1.000 1 2016 2016
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
Xeroderma Pigmentosum, Complementation Group D
0.010 1.000 1 2014 2014
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2016 2016
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
0.010 1.000 1 2015 2015
dbSNP: rs1799794
rs1799794
0.763 0.320 14 103712930 splice region variant T/C snv 0.22
CUI: C0023267
Disease: Fibroid Tumor
Fibroid Tumor
0.010 1.000 1 2015 2015