Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9444348
NT5E
6 85465856 intron variant G/A snv 0.43 2
rs10518133
PARM1
4 75025495 intron variant G/A snv 9.7E-02 1
rs16946160
GPC5
13 91551559 intron variant G/A snv 0.13 1
rs201899638
PTPRD
9 9932324 intron variant T/C;G snv 1
rs2637678 6 116466215 upstream gene variant T/C snv 0.36 1
rs2746419
AHI1
6 135332717 intron variant A/C snv 0.46 1
rs28366266
HLA-DRB1
6 32591976 upstream gene variant T/C snv 0.12 1
rs2858317 6 32694503 intergenic variant C/A snv 0.41 1
rs4431401
NT5E
6 85479802 intron variant T/C snv 0.46 1
rs4642516 6 32689766 TF binding site variant G/A;T snv 1
rs487575
LOC105374264
3 187880609 intergenic variant C/T snv 0.23 1
rs59882675
BTC
4 74763902 intron variant A/G snv 0.23 1
rs6020178
SNAI1
20 49987403 intron variant T/C snv 0.35 1
rs9273542
HLA-DQB1 ; HLA-DQB1-AS1
6 32661035 intron variant C/A;T snv 1
rs9348883
TSBP1-AS1 ; HCG23
6 32390772 non coding transcript exon variant T/A;G snv 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs28940578
MEFV
0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 16
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16