rs2981579, FGFR2

N. diseases: 8
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 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 9 2009 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 7 2009 2017
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.700 1.000 1 2010 2010
Oestrogen receptor positive breast cancer
58 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.700 1.000 1 2017 2017
Carcinoma of Male Breast
CUI: C0238033
Disease: Carcinoma of Male Breast
38 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.010 1.000 1 2011 2011
Lobular carcinoma in situ of breast
CUI: C0279563
Disease: Lobular carcinoma in situ of breast
4 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.010 1.000 1 2014 2014
Malignant neoplasm of male breast
CUI: C0242787
Disease: Malignant neoplasm of male breast
43 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.010 1.000 1 2011 2011
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.010 1.000 1 2019 2019