Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7158663
MEG3
0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 9
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs1414521156
SLCO6A1
5 102459731 missense variant T/A;C snv 4.0E-06; 4.0E-06 1
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
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
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
rs9583269
MYO16
0.790 0.080 13 108630682 intron variant C/T snv 0.34 9
rs770292690
TCHP
12 109908872 missense variant C/T snv 5.6E-05 9.8E-05 1
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
rs9481067
SLC22A16
0.776 0.080 6 110429349 intron variant A/G snv 0.58 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs4849303
ACOXL
0.790 0.080 2 110970905 intron variant C/G;T snv 9
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 10