Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 5
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 4
rs2471738
STH ; MAPT
0.882 0.160 17 45998697 intron variant C/T snv 0.18 4
rs4239633
UNC13A
0.851 0.240 19 17631660 intron variant C/T snv 0.32 4
rs1411478
STX6
0.925 0.120 1 180993146 intron variant A/G snv 0.56 3
rs1816
KANSL1
0.882 0.200 17 46199252 intron variant A/G snv 0.14 3
rs10675541
MOBP
1.000 0.120 3 39468795 intron variant -/CA delins 1
rs147124286
SP1
1.000 0.120 12 53394218 intron variant -/A delins 0.18 1
rs2045091
ASAP1
1.000 0.120 8 130063613 intron variant C/T snv 0.15 1
rs35740963
RUNX2
1.000 0.120 6 45531876 intron variant -/T delins 1
rs564309
TRIM11 ; MIR6742
1.000 0.120 1 228397861 intron variant C/A snv 0.11 1
rs57113693
STX6
1.000 0.120 1 180983158 intron variant C/T snv 0.56 1
rs621042
PIK3C2G
1.000 0.120 12 18636073 intron variant C/A snv 0.36 1
rs6547705
LOC105374846 ; CD8B
1.000 0.120 2 86817193 intron variant G/A snv 0.83 1
rs76970862
LINC02210-CRHR1
1.000 0.120 17 45709317 intron variant A/G snv 4.6E-02 1
rs7966334
SLCO1A2
1.000 0.120 12 21314281 intron variant C/G snv 0.95 1
rs13302855 0.882 0.200 9 27595997 intergenic variant C/T snv 7.5E-02 3
rs2142991 1.000 0.120 10 42845657 intergenic variant C/G;T snv 1
rs6852535 1.000 0.120 4 122557561 intergenic variant G/A snv 0.24 1
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 11
rs12125383 1.000 0.120 1 221995092 regulatory region variant G/A snv 0.14 1
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62