Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs430397
HSPA5
0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs1501899
CASR
0.790 0.240 3 122188481 intron variant A/G snv 0.62 8
rs2168101
LMO1 ; LOC105376536
0.827 0.200 11 8233861 intron variant C/A snv 0.24 7
rs2153977
MAGI3
0.807 0.240 1 113537449 intron variant C/T snv 0.28 6
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs2271338
ADGRL3
0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs57961569
MYCNOS ; MYCN
0.827 0.200 2 15939643 intron variant G/A;C snv 5
rs6435862
BARD1
0.827 0.160 2 214807822 intron variant G/A;C;T snv 5
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 4
rs11037575
HSD17B12
0.882 0.080 11 43706780 intron variant T/C snv 0.36 4
rs3768716
BARD1
0.851 0.080 2 214771070 intron variant T/C snv 0.16 4
rs6776706
RARB
0.851 0.080 3 25439731 intron variant T/A snv 0.27 4
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62 4
rs10055201
IL31RA
0.882 0.080 5 55865274 intron variant A/G snv 0.76 3