Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs768843272
TFR2
0.925 0.080 7 100629298 missense variant T/C snv 8.4E-05 7.7E-05 2
rs28940298
VHL
0.776 0.280 3 10149921 missense variant C/T snv 2.1E-04 1.0E-04 9
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs4150558
GTF2H1
0.882 0.040 11 18332808 non coding transcript exon variant T/A snv 8.7E-03 3
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs4645948
MYC ; CASC11
0.882 0.160 8 127736252 synonymous variant C/T snv 2.8E-02 3
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 6
rs3775296
TLR3
0.851 0.160 4 186076613 splice region variant C/A snv 0.18 0.18 6
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 4
rs10132552
MEG3
1.000 0.040 14 100834675 non coding transcript exon variant T/C snv 0.25 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 15
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188