Source: GWASDB

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: rs1219648
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 1.000 3 2007 2018
dbSNP: rs2981582
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 0.971 1 2007 2019
dbSNP: rs3135753
rs3135753
FGFR2
0.925 0.120 10 121521144 intron variant T/C snv 4.0E-03
CUI: C0018099
Disease: Gout
Gout 		0.800 1.000 1 2013 2013
dbSNP: rs2981578
rs2981578
FGFR2
0.925 0.080 10 121580797 intron variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.790 0.909 2 2007 2018
dbSNP: rs2420946
rs2420946
FGFR2
0.851 0.160 10 121591810 intron variant T/C snv 0.56
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.770 1.000 2 2007 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 3 2009 2017
dbSNP: rs3750817
rs3750817
FGFR2
0.851 0.080 10 121573063 intron variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.720 1.000 1 2009 2012
dbSNP: rs10736303
rs10736303
FGFR2
0.882 0.120 10 121574943 intron variant G/A snv 0.40
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.710 1.000 1 2007 2012
dbSNP: rs2981575
rs2981575
FGFR2
0.882 0.120 10 121586602 intron variant G/A snv 0.54
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.710 1.000 1 2007 2010
dbSNP: rs1219642
rs1219642
FGFR2
1.000 0.080 10 121588875 intron variant T/C snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 1.000 1 2007 2007
dbSNP: rs1219648
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs2912774
rs2912774
FGFR2
0.925 0.080 10 121589148 intron variant T/A;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 1.000 1 2007 2007
dbSNP: rs2936870
rs2936870
FGFR2
1.000 0.080 10 121589388 intron variant T/C snv 0.54
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 1.000 1 2007 2007
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: rs2981582
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010