Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs320995
CYSLTR1
0.851 0.240 X 78272820 missense variant G/A;C;T snv 0.73 4
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs2248359
CYP24A1
0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 8
rs2853209
ADAM33
0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs16999165 1.000 0.120 20 54190682 intergenic variant A/G snv 5.5E-02 1
rs4809219
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.120 20 63671762 intron variant C/A;G;T snv 1
rs909341
RTEL1-TNFRSF6B ; TNFRSF6B
1.000 0.120 20 63697389 synonymous variant C/T snv 0.25 0.19 1
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3
rs1221479287
KIR2DS1 ; KIR3DL1 ; KIR2DL1 ; KIR2DS4
0.925 0.120 19 54783499 missense variant G/A snv 7.0E-06 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs2164983 0.925 0.120 19 8679120 downstream gene variant C/A;G snv 0.19 2
rs3219177
RETN
0.925 0.120 19 7669483 intron variant C/T snv 0.20 0.19 2
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs436857
IL12RB1
0.925 0.120 19 18086825 5 prime UTR variant G/A snv 0.16 0.17 2
rs612529
VSTM1
0.925 0.120 19 54063999 upstream gene variant A/G;T snv 2
rs73510898
ZGLP1
0.925 0.120 19 10305768 intron variant G/A;C;T snv 2
rs2918307 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 1
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 5
rs4572450
ZNF652
0.882 0.120 17 49343367 intron variant T/C snv 0.78 4
rs11079788
TBX21
0.925 0.120 17 47743357 intron variant C/T snv 0.23 2