Gene: FGFR2 ×
Source: BEFREE ×
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: rs2981582
rs2981582
FGFR2
20 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.800 0.972 34 2007 2019
dbSNP: rs1219648
rs1219648
FGFR2
16 0.716 0.320 10 121586676 intron variant A/G;T snv 0.800 1.000 21 2007 2018
dbSNP: rs2981578
rs2981578
FGFR2
2 0.925 0.080 10 121580797 intron variant C/A;T snv 0.790 0.909 9 2009 2018
dbSNP: rs2420946
rs2420946
FGFR2
4 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 7 2009 2017
dbSNP: rs2981579
rs2981579
FGFR2
6 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 4 2009 2017
dbSNP: rs11200014
rs11200014
FGFR2
3 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 0.720 1.000 2 2012 2016
dbSNP: rs3750817
rs3750817
FGFR2
4 0.851 0.080 10 121573063 intron variant C/G;T snv 0.720 1.000 2 2009 2012
dbSNP: rs2981575
rs2981575
FGFR2
2 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.710 1.000 1 2010 2010
dbSNP: rs35054928
rs35054928
FGFR2
4 0.851 0.080 10 121580918 intron variant C/- delins 0.710 1.000 1 2016 2017
dbSNP: rs10736303
rs10736303
FGFR2
3 0.882 0.120 10 121574943 intron variant G/A snv 0.40 0.010 1.000 1 2012 2012
dbSNP: rs1078806
rs1078806
FGFR2
2 0.925 0.080 10 121579461 intron variant A/G;T snv 0.34 0.010 1.000 1 2008 2008
dbSNP: rs1296941849
rs1296941849
FGFR2
2 0.925 0.080 10 121496653 missense variant G/A snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs746116691
rs746116691
FGFR2
2 0.925 0.080 10 121515162 synonymous variant A/G;T snv 4.0E-06 0.010 < 0.001 1 2009 2009
dbSNP: rs774554190
rs774554190
FGFR2
2 0.925 0.080 10 121593750 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs779848635
rs779848635
FGFR2
4 0.925 0.080 10 121565562 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs7895676
rs7895676
FGFR2
2 0.925 0.080 10 121574483 intron variant C/T snv 0.40 0.010 < 0.001 1 2009 2009