Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs747093473
CDX2
1.000 0.080 13 27968819 missense variant G/A snv 7.0E-06 1
rs63750709
MSH2
0.925 0.160 2 47480846 missense variant C/G;T snv 4.0E-06 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
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 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
rs17033
ADH1B
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02 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
rs2289590
AURKB
0.925 0.080 17 8207446 intron variant C/A snv 0.54 2
rs11084490
AURKC
0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs758099
AURKC
0.925 0.080 19 57231966 intron variant C/G;T snv 2
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs384490
CARS1
0.925 0.080 11 3057655 splice region variant T/G snv 0.46 2
rs729662
CARS1
0.925 0.080 11 3006910 synonymous variant G/A snv 0.35 0.25 2
rs7394702
CARS1
0.925 0.080 11 3022918 intron variant T/C snv 0.17 2