rs1136201, ERBB2

N. diseases: 34
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Fibroadenoma
CUI: C0206650
Disease: Fibroadenoma
1 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2008 2008
HER2-negative breast cancer
CUI: C4733095
Disease: HER2-negative breast cancer
18 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2014 2014
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2005 2005
HER2-positive carcinoma of breast
CUI: C1960398
Disease: HER2-positive carcinoma of breast
26 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 1.000 2 2014 2015
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2008 2008
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2004 2004
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2005 2005
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2019 2019
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2019 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2016 2018
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2016 2018
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2008 2008
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2016 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2002 2019
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2016 2018