Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1452231640
POLB
1.000 0.080 8 42339015 missense variant T/C snv 4.0E-06 4
rs2294693
UNC5CL ; OARD1
1.000 0.080 6 41037763 intron variant T/C snv 0.26 3
rs121908382
MUTYH
1.000 0.080 1 45331530 missense variant G/A snv 2
rs121908383
MUTYH
1.000 0.080 1 45331502 missense variant T/C snv 2
rs121909776
CASP10
1.000 0.080 2 201187798 missense variant T/C snv 1.2E-04 2.8E-05 2
rs121912469
IRF1
1.000 0.080 5 132489457 missense variant T/A snv 2
rs2297882
MINDY3
1.000 0.080 10 15860304 5 prime UTR variant A/G snv 0.29 0.34 2
rs28933379
APC
1.000 0.080 5 112838953 missense variant G/A snv 2
rs10029005
LINC02516
1.000 0.080 4 124530209 intron variant G/A snv 0.40 1
rs10509671
PLCE1
1.000 0.080 10 94309297 intron variant T/G snv 0.24 1
rs1108143 1.000 0.080 2 234557214 regulatory region variant A/G snv 8.1E-02 1
rs1203145163
TFF1 ; LOC105372815
1.000 0.080 21 42363329 missense variant C/A snv 7.0E-06 1
rs1635566
PADI4
1.000 0.080 1 17356662 intron variant A/G snv 0.70 1
rs17042407 1.000 0.080 2 112801337 intergenic variant T/C snv 0.23 1
rs202208566
TCHP
1.000 0.080 12 109903156 missense variant T/C snv 6.5E-04 1.7E-04 1
rs367807476
STK11
1.000 0.080 19 1223035 missense variant C/G;T snv 9.2E-06 1.4E-05 1
rs372481703
APC
1.000 0.080 5 112839106 missense variant G/A snv 1.6E-05 1.4E-05 1
rs6897169
PTGER4 ; TTC33
1.000 0.080 5 40726036 intron variant C/A;T snv 0.24 1
rs7624041 1.000 0.080 3 94389819 intergenic variant G/A snv 0.89 1
rs7712641
LINC02161
1.000 0.080 5 89607147 intron variant T/A;C snv 1
rs7849280
ABO
1.000 0.080 9 133251249 non coding transcript exon variant A/G snv 1
rs80142782
ASH1L
1.000 0.080 1 155515236 intron variant T/C snv 2.9E-03 1
rs882537
PADI4
1.000 0.080 1 17333552 intron variant A/G snv 0.64 1
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs2269772
ITGA3
0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6