Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs7111520
POU2AF1
1.000 0.120 11 111378886 intron variant G/A snv 0.58 1
rs360719
IL18 ; LOC107987164 ; TEX12
0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 7
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
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
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs9482849 1.000 0.120 6 127967391 downstream gene variant T/C snv 0.14 1
rs752427
PVT1
1.000 0.120 8 127967762 intron variant C/T snv 0.55 1
rs4733809
PVT1
1.000 0.120 8 127977046 intron variant C/T snv 0.54 1
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27 2
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45