Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs35822372 0.776 0.160 2 88438931 intergenic variant C/A;T snv 8
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8
rs917412 0.776 0.160 4 108350621 TF binding site variant C/T snv 0.21 8
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv 8
rs4498834
CACNA1S
0.776 0.160 1 201111170 intron variant T/C snv 0.56 8
rs35956082
FOXP1
0.776 0.160 3 71414748 intron variant A/C;G snv 8
rs758468472
NOL11 ; LOC101928045
0.776 0.160 17 67718094 splice region variant G/T snv 8
rs121909636
FGFR1
0.827 0.240 8 38414569 stop gained G/A snv 7
rs121909635
FGFR1
0.827 0.240 8 38426158 missense variant C/T snv 6
rs267606805
FGFR1
0.851 0.240 8 38414173 missense variant G/T snv 5
rs267606806
FGFR1
0.851 0.240 8 38414166 missense variant G/A;C snv 1.2E-05 5
rs4904210
PAX9
0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 5
rs572007403
KISS1R
0.882 0.200 19 919955 missense variant C/A snv 3.3E-04 9.1E-05 4