Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6