Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1555206402
HMBS
0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins 26
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs2054576
ABCG2
0.882 0.160 4 88107623 intron variant A/G snv 7.8E-02 4
rs2544390
LRP2
0.925 0.080 2 169348336 intron variant C/T snv 0.45 4
rs2941484
HNF4G
0.882 0.160 8 75566533 3 prime UTR variant C/T snv 0.52 4
rs505802
SLC22A12
0.882 0.160 11 64589600 upstream gene variant T/C snv 0.45 4
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs11602903
SLC22A12
0.882 0.120 11 64590769 5 prime UTR variant A/T snv 0.51 3
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs475688
SLC22A12
0.882 0.160 11 64596819 intron variant C/T snv 0.25 3
rs7903456
SHLD2
0.882 0.160 10 87159562 intron variant C/T snv 0.69 3
rs893006
SLC22A12
0.882 0.160 11 64598324 intron variant C/A snv 0.61 3
rs1653624
P2RX7 ; LOC105370032
0.925 0.120 12 121184717 missense variant T/A snv 1.5E-02 2
rs1822825
PPARG
0.925 0.080 3 12408464 intron variant G/A snv 0.61 2
rs28934583
UMOD
0.925 0.240 16 20348652 missense variant A/C;G snv 2
rs6837293
PRKG2
0.925 0.160 4 81141777 intron variant C/A;T snv 2
rs7688672
PRKG2
0.925 0.160 4 81148295 intron variant G/A snv 0.39 2
rs1025993235
PRPSAP2
1.000 0.040 17 18865880 missense variant C/T snv 1
rs1230053514
SLC22A12
1.000 0.040 11 64598551 missense variant C/T snv 1
rs130154
TAFA5
1.000 0.040 22 48710770 intron variant C/T snv 0.69 1
rs4148500
ABCC4
1.000 0.040 13 95166034 intron variant G/A snv 1.9E-02 1