rs2420946, 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 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 9 2007 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 8 2009 2017
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.010 1.000 1 2012 2012
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.010 1.000 1 2019 2019