rs2981582, FGFR2

N. diseases: 21
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.800 0.972 36 2007 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.800 0.971 35 2007 2019
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.030 1.000 3 2012 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.030 1.000 3 2009 2012
Carcinoma of Male Breast
CUI: C0238033
Disease: Carcinoma of Male Breast
38 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.020 1.000 2 2013 2018
estrogen receptor-negative breast cancer
40 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.020 1.000 2 2011 2013
Malignant neoplasm of male breast
CUI: C0242787
Disease: Malignant neoplasm of male breast
43 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.020 1.000 2 2013 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.020 1.000 2 2012 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.020 1.000 2 2012 2019
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2019 2019
Early-Stage Breast Carcinoma
CUI: C2986665
Disease: Early-Stage Breast Carcinoma
7 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2013 2013
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2019 2019
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.700 1.000 1 2010 2010
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012
Node-negative breast cancer
CUI: C3160889
Disease: Node-negative breast cancer
2 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012
Non-Functioning Pituitary Gland Neoplasm
2 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2018 2018
Oestrogen receptor positive breast cancer
58 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2013 2013
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012