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: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma
Neoplasms 0.020 1.000 2 2012 2014
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular
Neoplasms 0.020 1.000 2 2012 2014
dbSNP: rs12494623
rs12494623
1.000 0.080 3 179214763 intron variant C/G;T snv
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
Cervical Squamous Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs1517586
rs1517586
3 179166120 intron variant T/C snv 7.1E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs1607237
rs1607237
1.000 0.040 3 179232509 intron variant C/T snv 0.68
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs17849071
rs17849071
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2677764
rs2677764
0.925 0.080 3 179206019 intron variant C/A;T snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs2677764
rs2677764
0.925 0.080 3 179206019 intron variant C/A;T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
Metastatic malignant neoplasm to brain
Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs2699887
rs2699887
0.763 0.280 3 179148620 intron variant C/T snv 0.18
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2699905
rs2699905
3 179166549 intron variant C/T snv 0.19
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019