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
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 15
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 6
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 4
rs987710
IGLV10-54
1.000 0.040 22 22158022 intron variant G/A snv 0.61 4
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs1531289
KDR
0.925 0.080 4 55089065 intron variant T/A;C snv 2
rs7072268
HK1
0.925 0.120 10 69340157 intron variant T/C snv 0.54 2
rs1375515
CACNA2D3
1.000 0.040 3 54442613 intron variant C/T snv 0.58 1
rs1868505
CACNA2D3
1.000 0.040 3 54387228 intron variant T/C snv 0.86 1
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs12762549 1.000 0.040 10 99861014 intergenic variant C/G;T snv 1
rs559063155
SF3B1
0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 14
rs33950507
HBB
0.807 0.080 11 5226943 stop gained C/A;G;T snv 2.5E-04 8
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226