Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 29
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 27
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 11
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 10
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 5
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 5
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 3
rs1057520029
FGFR2
0.925 0.120 10 121488003 missense variant T/A snv 3
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 3
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 2
rs121913477
FGFR2
1.000 0.120 10 121515289 missense variant G/C;T snv 1