Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs4889
KISS1
0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 5
rs1490384 6 126530014 intron variant C/G;T snv 4
rs1659127 16 14294448 intergenic variant G/A;C;T snv 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs4549631 6 126645162 intron variant T/C;G snv 3
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 3
rs1040070
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74512186 intron variant G/A;C snv 2
rs2090409
LINC01505
1.000 0.040 9 106204807 intron variant C/A;T snv 2
rs3115524
SYCE2 ; GCDH
19 12910545 intron variant G/A;C;T snv 2
rs35005436
GTF2I ; LOC101926943
1.000 0.080 7 74720592 intron variant C/A;G;T snv 2
rs643428
SSBP3
1 54263185 intron variant C/G;T snv 2
rs7161194
MIR541
14 101062668 upstream gene variant A/G;T snv 2
rs10019555
TACR3
4 103694124 intron variant G/A;C snv 1
rs10094574 8 77203831 intergenic variant G/A;T snv 1
rs10217747
ZNF483
9 111547655 3 prime UTR variant T/A;C snv 1
rs10401175
MAST3
19 18119464 intron variant C/A;G snv 1
rs10423674
CRTC1
19 18707093 intron variant C/A;T snv 1
rs10786610 10 100880906 TF binding site variant G/C;T snv 1