Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780759537
CDH1
1.000 0.080 16 68822082 missense variant G/A snv 1.6E-05 4.2E-05 1
rs747093473
CDX2
1.000 0.080 13 27968819 missense variant G/A snv 7.0E-06 1
rs768678989
MET
1.000 0.080 7 116771932 missense variant C/T snv 2.8E-05 1
rs771333219
MET
1.000 0.080 7 116759444 missense variant C/T snv 1.2E-04 8.4E-05 1
rs63749803
MLH1
1.000 0.080 3 37004421 missense variant T/C;G snv 1
rs63750297
MLH1
1.000 0.080 3 37004412 missense variant C/A;G;T snv 8.0E-06 1
rs63751047
MLH1
1.000 0.080 3 37048525 missense variant C/A;G snv 1
rs63750795
MSH2
1.000 0.080 2 47480854 missense variant T/G snv 1
rs63750966
MSH2
1.000 0.080 2 47403240 missense variant G/A;C;T snv 1
rs63751400
MSH2
1.000 0.080 2 47480839 missense variant C/G;T snv 4.0E-06 1
rs1371429276
PTPRT
1.000 0.080 20 42472359 missense variant G/A snv 1.4E-05 1
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs1887427 0.925 0.080 9 4979730 upstream gene variant A/G snv 0.21 2
rs1892901 0.925 0.080 11 65903422 upstream gene variant G/A snv 9.5E-03 2
rs26160 0.925 0.080 5 145353893 intron variant T/C snv 4.5E-03 2
rs36012910 0.925 0.080 2 25345310 upstream gene variant A/C;G snv 2
rs4145643 0.925 0.080 10 60803097 regulatory region variant G/C;T snv 2
rs283411
ADH1C ; ADH1B
0.925 0.080 4 99344800 intron variant C/A;T snv 2
rs16941667
ALDH2
0.925 0.080 12 111806609 intron variant C/T snv 8.6E-02 2
rs1279599
AMD1
0.925 0.080 6 110879025 intron variant G/A snv 0.87 2
rs7768897
AMD1
0.925 0.080 6 110891080 non coding transcript exon variant A/G;T snv 2
rs2279284
ARNTL
0.925 0.080 11 13277203 intron variant C/T snv 0.25 2
rs911160
AURKA
0.925 0.080 20 56382507 intron variant G/A;C snv 2
rs2241909
AURKB
0.925 0.080 17 8205021 synonymous variant G/A snv 0.66 0.64 2