Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs892295
CHL1
3 355870 intron variant A/G snv 0.87 4
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs1998303 9 82800066 intergenic variant A/G snv 0.37 3
rs73186036
N6AMT1
21 28754160 regulatory region variant A/G snv 0.20 2
rs9436480
CDCP2
1 54151583 intron variant A/G snv 8.9E-02 2
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3
rs4896310
LOC105378021
1.000 0.120 6 138018697 intergenic variant A/G;T snv 3
rs2383733 9 27869512 intergenic variant A/G;T snv 2
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs13395911
EFHD1
2 232655544 intron variant A/T snv 0.59 3
rs34531324
LINC01411
1.000 0.120 5 174435441 intron variant A/T snv 0.16 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 6
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs13247499
JAZF1
7 28139639 intron variant C/A snv 0.10 2
rs754465
DLG5
10 77920756 intron variant C/A snv 0.52 2
rs200088103
GPT ; LOC101928953
8 144505033 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.0E-04 2
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3
rs1658972 9 6665010 intron variant C/A;T snv 2