Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4791171
AXIN2
0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs3130
PROM1 ; FGFBP2
0.882 0.080 4 15968315 3 prime UTR variant T/A;C snv 6
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 6
rs5273
PTGS2
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 5
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs1233296947
CTNNB1
0.851 0.080 3 41225746 missense variant G/A snv 4.0E-06 5
rs1289280947
CDKN2A
0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs146639652
POLE
0.827 0.080 12 132675752 missense variant G/A;C snv 1.2E-05 5
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 5
rs35301225
MIR34A ; MIR34AHG
0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs587777627
POLD1
0.807 0.080 19 50406444 missense variant T/C snv 5
rs6973569
NPSR1-AS1
0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 5
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs1044471
ADIPOR2
1.000 0.080 12 1787790 3 prime UTR variant C/T snv 0.38 4
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1064795747
MSH2
0.925 0.080 2 47412433 missense variant T/C snv 4
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4