Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071214
BIRC5
17 78223510 missense variant G/A snv 0.93 0.96 3
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs3816747
DLC1
1.000 0.080 8 13499293 missense variant G/A snv 0.87 0.89 2
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs6082527 20 2256129 intron variant G/A snv 0.88 1
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs2929973
CCN4
0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs822391
ADIPOQ
0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs11203495
DLC1
8 13499310 missense variant T/G snv 0.85; 4.0E-06 0.85 1
rs162561
CYP1B1
2 38071734 intron variant T/G snv 0.85 1
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 3
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 12
rs2479717
CCND3
0.925 0.080 6 41937436 intron variant T/A snv 0.79 0.81 3
rs738792
MMP11
0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs329007
RALBP1
18 9522608 intron variant G/A snv 0.79 1
rs14304
CCL18
1.000 0.080 17 36071135 3 prime UTR variant T/C snv 0.78 2
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs2306969
LOC101928844 ; FUT3
0.925 0.040 19 5851790 intron variant A/G snv 0.76 4
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6