rs2981575, FGFR2

N. diseases: 4
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.
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.710 1.000 2 2007 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.710 1.000 1 2010 2010
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018