Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs12442054 0.882 0.080 15 74165683 intron variant G/A snv 0.12 3
rs4758051 0.882 0.080 11 8217092 intergenic variant G/A snv 0.42 3
rs729147
ADH7
0.882 0.080 4 99412110 downstream gene variant G/A snv 0.78 3
rs773249771
ADRA1A
0.882 0.080 8 26864314 missense variant T/C snv 1.2E-05 3
rs1442511697
ADRA2B
0.882 0.080 2 96115494 missense variant T/C snv 7.0E-06 3
rs771723690
ARHGAP24
0.882 0.080 4 85570622 synonymous variant G/A snv 1.6E-05 3
rs17487792
BARD1
0.882 0.080 2 214778776 intron variant C/T snv 0.16 3
rs3738888
BARD1
0.882 0.080 2 214730440 missense variant G/A;T snv 8.4E-03 3
rs3768707
BARD1
0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs4712653
CASC15
0.882 0.080 6 22125735 intron variant T/C;G snv 3
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3
rs143864187
CASP4
0.882 0.080 11 104949666 missense variant C/A snv 3
rs1301478248
CASP9
0.882 0.080 1 15495395 missense variant C/T snv 3
rs3796725
CPZ ; GPR78
0.882 0.080 4 8616210 intron variant C/T snv 0.23 3
rs2619046
DDX4
0.882 0.080 5 55801706 intron variant G/A snv 0.34 3
rs758594231
DDX58
0.882 0.080 9 32500886 missense variant C/T snv 4.0E-06 3
rs1211164799
DLX4
0.882 0.080 17 49973938 missense variant A/T snv 3
rs867182279
EGFR
0.882 0.080 7 55205510 missense variant T/C snv 3
rs3796727
GPR78 ; CPZ
0.882 0.080 4 8611299 intron variant G/A snv 0.26 0.32 3
rs10055201
IL31RA
0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs145976111
ITGB4
0.882 0.080 17 75742728 missense variant C/T snv 2.9E-03 2.3E-03 3
rs147480547
ITGB4
0.882 0.080 17 75740047 missense variant G/A;T snv 1.1E-03; 4.0E-06 3
rs80059929
KIF15
0.882 0.080 3 44805230 intron variant T/A snv 3.6E-02 3