Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs619586
MALAT1
0.724 0.360 11 65498698 non coding transcript exon variant A/G snv 5.9E-02 3.3E-02 15
rs5743704
TLR2
0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs137852741
BMPR2
0.807 0.120 2 202556360 stop gained C/G;T snv 4.0E-06 7
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs886039303
STAMBPL1 ; ACTA2
0.882 0.160 10 88941310 missense variant G/A snv 5
rs1085307252
BMPR2
0.882 0.080 2 202518890 missense variant A/T snv 3
rs1085307253
BMPR2
0.882 0.080 2 202518890 frameshift variant AG/T delins 3
rs137852749
BMPR2
0.882 0.080 2 202552774 missense variant G/A snv 3
rs863223746
SMAD3
0.925 0.080 15 67187472 missense variant C/T snv 3
rs10744676
KCNA5
0.925 0.080 12 5043783 upstream gene variant C/T snv 0.88 2
rs201234174
MUC6
0.925 0.080 11 1017655 missense variant G/A snv 4.0E-02 3.0E-02 2
rs374514431
NFU1
0.925 0.040 2 69400462 missense variant C/A snv 1.5E-04 1.2E-04 2
rs367837827
VARS2
0.925 0.080 6 30922159 missense variant C/T snv 1.9E-04 7.7E-05 2
rs775921458
ABCC8
1.000 0.040 11 17407404 missense variant C/T snv 3.2E-05 4.9E-05 1
rs2277382
ACVRL1
1.000 0.040 12 51912437 missense variant C/T snv 8.4E-02 7.7E-02 1
rs41322046
ENG ; LOC105379841
1.000 0.040 9 127825812 missense variant C/T snv 8.8E-03 9.9E-03 1
rs1359984100
NOS3
1.000 0.040 7 151010603 stop gained C/T snv 7.0E-06 1