Source: ALL
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: rs121913476
rs121913476
FGFR2
7 0.851 0.080 10 121498520 missense variant A/C;T snv 0.700 1.000 4 2008 2013
dbSNP: rs79184941
rs79184941
FGFR2
41 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.700 1.000 3 2008 2012
dbSNP: rs1057519045
rs1057519045
FGFR2
6 0.851 0.160 10 121498522 missense variant T/G snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519794
rs1057519794
EGFR
2 0.925 0.080 7 55173927 missense variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs1057519795
rs1057519795
FGFR2
1 1.000 10 121488002 missense variant T/C snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519796
rs1057519796
FGFR2
1 1.000 10 121496546 missense variant A/T snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519797
rs1057519797
FGFR2
1 1.000 10 121496705 missense variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519798
rs1057519798
FGFR2
1 1.000 10 121498528 missense variant T/C snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519799
rs1057519799
FGFR2
1 1.000 10 121498556 missense variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519800
rs1057519800
FGFR2
1 1.000 10 121498562 missense variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519801
rs1057519801
PIK3R2
1 1.000 19 18167251 missense variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs121918506
rs121918506
FGFR2
3 0.882 0.080 10 121496701 missense variant T/C;G snv 0.700 1.000 1 2013 2013