Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs5070
APOA1 ; APOA1-AS
0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs243327
RMI2 ; LOC105371082
0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs33932899
LOC105371082 ; RMI2 ; SOCS1
0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 4
rs8048002
LOC112267907 ; CIITA
0.851 0.320 16 10898131 intron variant T/A;C snv 4
rs2029253
ALOX5
0.925 0.200 10 45396036 intron variant A/G snv 0.37 3
rs2046934
MED12L ; P2RY12
0.882 0.200 3 151339854 intron variant G/A;C snv 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs2240419
HDAC9
0.925 0.200 7 18935566 intron variant T/A;C snv 3
rs2389995
HDAC9
0.925 0.200 7 18933395 intron variant A/G snv 6.0E-02 3
rs2762939
CYP24A1
0.925 0.160 20 54164712 intron variant G/C;T snv 3
rs41273215
PEAR1
0.882 0.160 1 156912167 intron variant C/T snv 0.13 3
rs622064
DNAJB13
0.882 0.240 11 73961529 intron variant C/A snv 0.30 3
rs676457
ABO
1.000 0.120 9 133270797 intron variant T/A snv 3
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs2298212
TNFRSF4
0.925 0.200 1 1211917 intron variant G/A snv 8.3E-02 8.0E-02 2
rs33977706
RMI2 ; SOCS1 ; LOC105371082
0.925 0.200 16 11256298 intron variant C/A;G;T snv 2
rs3784929
KARS1
0.925 0.160 16 75643129 intron variant A/G snv 0.30 2
rs9508835
ALOX5AP
1.000 0.120 13 30760561 intron variant C/A snv 0.23 1
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2075252
LRP2
0.925 0.160 2 169154475 stop gained T/A;C snv 0.76 5