Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs144610914
PIBF1
0.882 0.240 13 72908550 missense variant A/G snv 5.8E-05 2.1E-05 3
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
rs911707459
PIBF1
0.925 0.120 13 72965358 missense variant A/T snv 7.0E-06 2