Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520027
FGFR2
10 121488005 missense variant T/C snv 1
rs1057520028
FGFR2
10 121515283 missense variant T/C snv 1
rs121913475
FGFR2
10 121519989 missense variant T/C snv 1
rs121913477
FGFR2
1.000 0.120 10 121515289 missense variant G/C;T snv 2
rs1057520029
FGFR2
0.925 0.120 10 121488003 missense variant T/A snv 4
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
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
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13