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: rs35054928
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.710 1.000 2 2016 2017
dbSNP: rs35054928
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2016 2016
dbSNP: rs35054928
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins
CUI: C3642346
Disease: Luminal B Breast Carcinoma
Luminal B Breast Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs35054928
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins
CUI: C3642345
Disease: Luminal A Breast Carcinoma
Luminal A Breast Carcinoma 		0.010 1.000 1 2017 2017