Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4142986
COL15A1
0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs755725121
PIK3CD
0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs499952
MRE11
0.925 0.040 11 94449826 intron variant G/T snv 0.41 2
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs2155209
MRE11
0.776 0.240 11 94417624 3 prime UTR variant T/C snv 0.27 10
rs1314386070
DECR1
0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs749582333
NOX4
0.925 0.040 11 89340157 frameshift variant G/- delins 2
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4754
SPP1
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs8070488
HGS
0.882 0.080 17 81696901 synonymous variant T/C snv 0.21 0.26 3
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 7
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs1403934301
SHBG
0.882 0.120 17 7631317 missense variant G/A snv 3