Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs11655237
LINC00511 ; LINC00673
0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs1057519865
FOXL2NB ; FOXL2
0.742 0.240 3 138946321 missense variant G/C snv 15
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs2276466
ERCC4
0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1285136498
NR3C1
0.807 0.080 5 143400101 missense variant G/A snv 13