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
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs6749704
CCL20
0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs12817819
ATP2B1
0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 3
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs4782371
ZFPM1
1.000 0.040 16 88502423 intron variant T/A;G snv 3
rs17105278
RAD51B
0.925 0.080 14 68261762 intron variant T/C snv 0.36 2
rs2639990
ZADH2
1.000 0.040 18 75203596 intron variant T/C snv 0.12 2
rs7043199
VLDLR ; VLDLR-AS1
1.000 0.040 9 2621145 intron variant T/A snv 0.18 2
rs3917643
F3
1.000 0.040 1 94536311 intron variant T/C snv 3.9E-02 1