Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs10145099
TSHR
1.000 0.120 14 80990350 intron variant C/T snv 0.35 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10197319 1.000 0.120 2 203898321 regulatory region variant G/A;T snv 1
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044043
TAP2
1.000 0.120 6 32826204 3 prime UTR variant A/C snv 0.82 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs1061501
IRF7
0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs1061502
IRF7
0.882 0.160 11 614318 missense variant T/C snv 0.25 0.33 3
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs10760130 0.925 0.200 9 120939712 intergenic variant G/A snv 0.45 2
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs10908583 1.000 0.120 1 157671893 downstream gene variant C/T snv 0.57 1
rs111033243
SLC26A4
0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs111033304
SLC26A4
1.000 0.120 7 107683334 missense variant A/C;G snv 1.0E-03 1
rs11166985
AGO2
1.000 0.120 8 140634077 intron variant A/G snv 0.71 1
rs11171806
IL23A
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 7
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16