Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 6
rs2732260
FUT10
0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 5
rs4239633
UNC13A
0.851 0.240 19 17631660 intron variant C/T snv 0.32 4
rs4877365
DAPK1
0.851 0.120 9 87540777 intron variant G/A snv 0.28 4
rs4878104
DAPK1
0.851 0.120 9 87578076 intron variant C/T snv 0.40 4
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs1816
KANSL1
0.882 0.200 17 46199252 intron variant A/G snv 0.14 3
rs12546767
WASHC5
0.925 0.120 8 125070323 intron variant T/C;G snv 2
rs1358071
LINC02210-CRHR1
1.000 0.120 17 45725823 intron variant C/A;T snv 2
rs302668
RAB38
0.925 0.120 11 88143743 intron variant T/C snv 0.28 2
rs538622
ERGIC1
0.925 0.120 5 172920676 intron variant A/G snv 0.40 2
rs13393316
NDUFS1
1.000 0.120 2 206134615 intron variant A/G snv 0.14 1
rs17042852
LINC01867 ; LOC730100
1.000 0.120 2 52372929 intron variant T/C snv 3.0E-02 1
rs2659030
CEP131
1.000 0.120 17 81204174 intron variant G/A;T snv 0.36 1
rs2725391
CEP131
1.000 0.120 17 81218630 intron variant C/T snv 0.37 1
rs36196656
GFRA2
1.000 0.120 8 21763735 intron variant C/A;G;T snv 1
rs6108746 1.000 0.120 20 10922123 intron variant T/C snv 0.16 1
rs63750308
MAPT
1.000 0.120 17 46010415 intron variant A/G snv 1
rs63750972
MAPT
1.000 0.120 17 46010416 intron variant C/T snv 1
rs63751394
MAPT
1.000 0.120 17 46010413 intron variant T/C snv 1
rs6809184
TNIK
1.000 0.120 3 171170409 intron variant C/T snv 6.2E-02 1
rs6962939
COL28A1
1.000 0.120 7 7484595 intron variant T/A snv 5.4E-02 1
rs7240419
ATP9B
1.000 0.120 18 79168989 intron variant G/A snv 0.24 1