Gene: FGFR2 ×
Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1219648
rs1219648
FGFR2
1 0.716 0.320 10 121586676 intron variant A/G;T snv 0.800 1.000 4 2007 2018
dbSNP: rs2981582
rs2981582
FGFR2
1 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.800 0.972 2 2007 2019
dbSNP: rs2981578
rs2981578
FGFR2
1 0.925 0.080 10 121580797 intron variant C/A;T snv 0.790 0.909 2 2009 2018
dbSNP: rs2420946
rs2420946
FGFR2
1 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 1 2009 2017
dbSNP: rs2981579
rs2981579
FGFR2
2 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 5 2009 2017
dbSNP: rs11200014
rs11200014
FGFR2
17 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 0.720 1.000 1 2012 2016
dbSNP: rs3750817
rs3750817
FGFR2
1 0.851 0.080 10 121573063 intron variant C/G;T snv 0.720 1.000 1 2009 2012
dbSNP: rs2981575
rs2981575
FGFR2
3 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.710 1.000 1 2010 2010
dbSNP: rs35054928
rs35054928
FGFR2
1 0.851 0.080 10 121580918 intron variant C/- delins 0.710 1.000 1 2016 2017
dbSNP: rs10510097
rs10510097
FGFR2
1 1.000 0.080 10 121568362 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs2912774
rs2912774
FGFR2
1 0.925 0.080 10 121589148 intron variant T/A;G snv 0.700 1.000 1 2014 2014
dbSNP: rs3135718
rs3135718
FGFR2
2 0.882 0.160 10 121594355 intron variant C/T snv 0.54 0.700 1.000 1 2016 2016
dbSNP: rs3135724
rs3135724
FGFR2
2 1.000 0.080 10 121592706 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs45631563
rs45631563
FGFR2
1 1.000 0.080 10 121589810 intron variant A/T snv 3.6E-02 0.700 1.000 1 2017 2017