Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3213172
E2F1
0.882 0.080 20 33677511 missense variant C/T snv 2.4E-05 2.1E-05 3
rs2862833
FAS
0.882 0.080 10 89015872 3 prime UTR variant A/G snv 0.45 3
rs9513111
FLT1
0.882 0.080 13 28423426 intron variant C/T snv 0.75 3
rs281860374
HLA-B ; HLA-C
0.882 0.080 6 31271730 missense variant G/C snv 3
rs3117027
HLA-DPB2
0.882 0.080 6 33121846 intron variant C/A;G snv 3
rs9272143
HLA-DQA1
0.882 0.080 6 32633026 intron variant T/C snv 0.49 3
rs12349785
INSL6 ; JAK2
0.882 0.080 9 5076613 intron variant G/C snv 0.23 3
rs10815144
JAK2 ; INSL6
0.882 0.080 9 5010192 intron variant G/A snv 0.62 3
rs77381814
KLC1 ; XRCC3
0.882 0.080 14 103699410 missense variant C/T snv 1.5E-03 5.9E-03 3
rs4604006
LOC105377555 ; VEGFC
0.882 0.080 4 176687621 intron variant T/C snv 0.58 3
rs1003897973
LOC107985302 ; TRIP10
0.882 0.080 19 6746039 missense variant C/G snv 3
rs67841474
MICA
0.882 0.080 6 31412384 frameshift variant G/-;GG delins 0.21 0.19 3
rs10426502
MYDGF ; TNFAIP8L1
0.882 0.080 19 4651257 intron variant G/A snv 6.8E-02 3
rs1048512
PIGM ; KCNJ10
0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 3
rs1045935
PWAR6 ; SNHG14
0.882 0.080 15 25036439 non coding transcript exon variant G/A;T snv 3
rs2732044
PWAR6 ; SNHG14
0.882 0.080 15 25032169 non coding transcript exon variant G/A snv 0.34 3
rs3094
RNASE4
0.882 0.080 14 20699896 3 prime UTR variant T/C snv 0.18 3
rs1030389
SNHG14 ; PWAR6
0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 3
rs300574
SPRY1
0.882 0.080 4 123402583 3 prime UTR variant T/C snv 0.58 0.54 3
rs4728
SPRY2
0.882 0.080 13 80336651 3 prime UTR variant C/A;T snv 0.69; 7.0E-06 3
rs201567874
TGFB1
1.000 0.080 19 41348412 missense variant C/T snv 6.8E-05 5.6E-05 3
rs9917028
TNFAIP8L1
0.882 0.080 19 4640971 non coding transcript exon variant G/A snv 0.45 3
rs1060555
TNFAIP8L1 ; MYDGF
0.882 0.080 19 4652810 3 prime UTR variant C/G;T snv 3
rs944309752
TP53BP1
0.882 0.080 15 43421159 synonymous variant G/C snv 7.0E-06 3
rs12646659
VEGFC
0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02 3