Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34713741
SELENOS
0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs770917264
MOK
1.000 0.120 14 102229547 stop gained G/A;C snv 4.0E-06; 1.6E-05 1
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs1249910 1.000 0.120 3 112672327 intergenic variant A/G snv 0.58 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6997279
SLC30A8
0.882 0.160 8 116961613 intron variant G/T snv 0.20 3
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174