Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs2229546
IL12RB2
1.000 0.080 1 67395837 synonymous variant C/A;G;T snv 0.63; 1.2E-05; 2.4E-05 1
rs4297265
IL12RB2
1.000 0.080 1 67386652 synonymous variant G/A;T snv 1
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs750553272
NFE2L2
0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs12494623
PIK3CA
1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs3729679
PIK3CA
1.000 0.080 3 179204642 intron variant A/G snv 0.58 1
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs4705343
MIR143 ; CARMN
0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs3181224
LOC105377683
1.000 0.080 5 159313842 intron variant A/G snv 0.10 1
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs2229634
ITPR3
0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs3748079
ITPR3
0.925 0.160 6 33620370 5 prime UTR variant C/T snv 0.18 2
rs853360
CD83
1.000 0.080 6 14134361 intron variant T/C snv 0.74 1
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7