Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs104894630
SCO1
0.882 0.120 17 10692805 missense variant G/A snv 4
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs111200466
TLR2
1.000 0.080 4 153684312 5 prime UTR variant CGGCTGCTCGGCGTTCTCTCAGG/- delins 0.17 2
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs11554495
KRT8
0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs121434622
FMR1
1.000 0.080 X 147936534 missense variant T/A snv 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs1281032650
LNPEP
5 96979168 missense variant A/G snv 1
rs1290547844
BRD4
19 15273041 missense variant C/T snv 4.0E-06 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs1316569885
SORBS1
10 95399139 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1325863623
SERPINB6
6 2953175 missense variant C/T snv 4.0E-06 1
rs1371149614
SHBG
1.000 0.040 17 7630488 missense variant G/C snv 4.0E-06 2