Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.740 1.000 9 2009 2017
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.740 1.000 7 2009 2017
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C2938924
Disease: Oestrogen receptor positive breast cancer
Oestrogen receptor positive breast cancer 		0.700 1.000 1 2017 2017
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 1.000 1 2019 2019
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0279563
Disease: Lobular carcinoma in situ of breast
Lobular carcinoma in situ of breast 		0.010 1.000 1 2014 2014
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast 		0.010 1.000 1 2011 2011
dbSNP: rs2981579
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53
CUI: C0242787
Disease: Malignant neoplasm of male breast
Malignant neoplasm of male breast 		0.010 1.000 1 2011 2011