Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
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
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
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
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 4
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
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 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