Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10445371
MAPT
0.925 0.120 17 45988044 intron variant G/A snv 0.15 3
rs1078268
STH ; MAPT
0.925 0.120 17 45998535 intron variant A/G snv 0.15 3
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 3
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12449852
CDK12
1.000 0.080 17 39475835 intron variant A/G snv 0.79 3
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 3
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 3
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs17571739
MAPT
0.925 0.120 17 45955549 intron variant T/C snv 0.14 3
rs17571809
MAPT
0.925 0.120 17 45957493 intron variant A/G snv 0.14 3
rs17572169
MAPT
0.925 0.120 17 45968608 intron variant C/T snv 0.14 3
rs17577094
KANSL1
0.925 0.120 17 46110126 intron variant A/G snv 0.14 3
rs17649641
MAPT ; LOC105371800
0.925 0.120 17 45920006 intron variant T/C snv 0.14 3
rs17690679
SPPL2C ; MAPT-AS1
0.925 0.120 17 45847437 intron variant A/G snv 0.14 3
rs17769490
MAPT-AS1
0.925 0.120 17 45848239 intron variant G/A snv 0.14 3
rs17769552
MAPT-AS1
0.925 0.120 17 45849924 intron variant G/A snv 0.14 3
rs199515
WNT3 ; LRRC37A2
0.925 0.120 17 46779275 intron variant G/C snv 0.84 3
rs199525
WNT3 ; LRRC37A2
1.000 0.080 17 46770468 intron variant T/A;G snv 3
rs2293370
TIMMDC1
0.882 0.160 3 119501087 intron variant G/A snv 0.18 3
rs2300747
MIR548AC ; CD58
0.882 0.200 1 116561593 intron variant A/G snv 0.19 3
rs230534
NFKB1
0.882 0.120 4 102527884 intron variant T/C snv 0.73 3
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs2843403
MMEL1
0.882 0.200 1 2597658 intron variant T/C snv 0.54 3