Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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 5
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
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42 4
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs1007934
ZFYVE1
14 72996771 intron variant G/A snv 0.33 3
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs11688767
ACTG1P22
0.925 0.040 2 57761059 intron variant A/T snv 0.40 3