Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10883371
LINC01475 ; NKX2-3
1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 1
rs10905718 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 1
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11554825
GPBAR1
0.882 0.120 2 218261086 5 prime UTR variant C/T snv 0.44 3
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 6
rs12479056
PUS10
1.000 0.040 2 60948177 synonymous variant T/C snv 0.56 0.62 1
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 2
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs13191240
ADGRB3
1.000 0.040 6 68965567 intron variant T/C snv 4.5E-02 1
rs1452787
TCF4
0.827 0.160 18 55539976 intron variant A/G snv 0.24 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17683107
GAS7
1.000 0.040 17 9921085 intron variant G/A snv 0.13 1
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 2
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs213950
CFTR-AS1 ; CFTR
0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 4
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs3134883
IL2RA
1.000 0.040 10 6058762 intron variant G/A snv 0.23 1