Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386833760
CC2D2A
0.790 0.360 4 15587929 splice donor variant G/- delins 1.9E-04 11
rs886039792
TXNDC15
0.807 0.280 5 134874531 splice donor variant G/A snv 9
rs1553827236
CC2D2A
0.882 0.200 4 15516757 splice donor variant G/A snv 7
rs202676
FOLH1
0.851 0.160 11 49206068 stop lost A/G snv 0.28 0.33 7
rs2486668
GRHL3
0.807 0.320 1 24331573 missense variant C/G snv 0.16 0.17 6
rs10786691
SUFU
0.925 0.160 10 102604895 intron variant G/A;T snv 3
rs34396413
TFAP2A
0.925 0.160 6 10400802 intron variant AGA/- delins 6.8E-02 6.9E-02 3