Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 17
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs1512436 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 10
rs17035310 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 10
rs4727012 0.790 0.080 7 149043401 intergenic variant C/T snv 0.12 10
rs76225372 0.790 0.080 10 19031157 intergenic variant A/G snv 7.4E-02 10
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs6051080
FAM182A
0.790 0.080 20 25995038 intron variant A/G snv 0.48 10
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs4378954
LSAMP
0.790 0.080 3 115931601 intron variant T/C snv 0.83 10
rs9901225
RETREG3
0.790 0.080 17 42603793 intron variant C/G;T snv 10
rs17503919
RNGTT
0.790 0.080 6 88856018 intron variant A/G snv 9.4E-02 10
rs7740797
SCAF8
0.790 0.080 6 154800125 intron variant G/C snv 0.62 10
rs3181245
TDP2
0.790 0.080 6 24651092 intron variant C/G snv 0.42 0.46 10
rs2052678
TMTC1
0.790 0.080 12 29680396 intron variant G/A snv 0.21 10
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6