Gene: FGFR2 ×
Source: INFERRED ×
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: rs121918492
rs121918492
FGFR2
2 0.882 0.080 10 121517372 missense variant G/C snv 7.0E-06 0.810 1.000 0 1994 1998
dbSNP: rs776587763
rs776587763
FGFR2
6 0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.800 1.000 5 1994 2014
dbSNP: rs121918488
rs121918488
FGFR2
4 0.790 0.120 10 121517379 missense variant A/C;G;T snv 0.800 1.000 0 1994 1998
dbSNP: rs121918497
rs121918497
FGFR2
3 0.776 0.160 10 121520052 missense variant T/G snv 0.800 1.000 0 1994 1998
dbSNP: rs121918490
rs121918490
FGFR2
5 0.851 0.080 10 121517342 missense variant G/C snv 0.710 1.000 12 1994 2016
dbSNP: rs121918487
rs121918487
FGFR2
24 0.716 0.440 10 121517378 missense variant C/A;G;T snv 0.700 1.000 8 1994 2015
dbSNP: rs1057519044
rs1057519044
FGFR2
11 0.752 0.440 10 121517390 missense variant C/T snv 0.700 0
dbSNP: rs121913478
rs121913478
FGFR2
13 0.708 0.640 10 121515280 missense variant T/C snv 0.700 0
dbSNP: rs121918491
rs121918491
FGFR2
14 0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1434545235
rs1434545235
FGFR2
11 0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs1554927408
rs1554927408
FGFR2
11 0.742 0.480 10 121515254 missense variant C/T snv 0.700 0
dbSNP: rs77543610
rs77543610
FGFR2
12 0.667 0.560 10 121520160 missense variant G/C snv 0.700 0
dbSNP: rs79184941
rs79184941
FGFR2
18 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.700 0