Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 14
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1254244346
ABCA1
1.000 0.080 9 104822502 missense variant G/A snv 4.0E-06 1
rs17035289 0.790 0.080 4 105127134 intergenic variant T/C snv 0.25 9
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs17035310 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 10
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs6928864 0.790 0.080 6 105519019 intron variant C/A;T snv 9
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs1512436 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 10
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs587779858
ATM
1.000 0.080 11 108227692 missense variant G/A snv 1
rs772821016
ATM
0.882 0.320 11 108244873 stop gained C/T snv 4.0E-06 4
rs138398778
ATM
1.000 0.080 11 108247071 missense variant C/A;T snv 8.0E-06; 8.8E-05 1
rs202160435
ATM
0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 2
rs730881315
ATM ; C11orf65
1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-06 1
rs587782310
C11orf65 ; ATM
1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 1
rs587782652
ATM ; C11orf65
0.851 0.320 11 108335105 missense variant T/C snv 3.2E-05 4.2E-05 5
rs9583269
MYO16
0.790 0.080 13 108630682 intron variant C/T snv 0.34 9
rs7993934
COL4A2
0.790 0.080 13 110422568 intron variant C/T snv 0.56 9
rs8000189
COL4A2
0.776 0.080 13 110423534 intron variant C/T snv 0.61 10