Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 5
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 4
rs10498730
SLC17A1
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02 4
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 4