Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs10146249
ATXN3
1.000 0.080 14 92074996 intron variant C/A snv 0.29 1
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs137853590
PHKG2
0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 3
rs7158733
ATXN3
1.000 0.080 14 92070879 stop gained G/A;T snv 1.2E-05; 0.27 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100