Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs9585056
LOC107984558
1.000 0.120 13 99429512 non coding transcript exon variant C/G;T snv 1
rs10786436
HPSE2
1.000 0.120 10 98540425 intron variant C/T snv 0.40 1
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 4
rs1456988 0.925 0.160 14 98021670 intergenic variant G/T snv 0.61 2
rs3176792
CD69
1.000 0.120 12 9758491 intron variant A/T snv 6.8E-02 1
rs4763879
CD69
0.925 0.160 12 9757568 intron variant G/A snv 0.28 2
rs917911
CD69
1.000 0.120 12 9753255 3 prime UTR variant A/C snv 0.29 1
rs10492166
CLECL1
1.000 0.120 12 9733403 upstream gene variant G/A snv 0.50 1
rs11052552
LINC02390
1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42 1
rs16919034
CTSV
1.000 0.120 9 97031301 3 prime UTR variant A/G snv 0.28 1
rs2762
LNPEP ; ERAP1
1.000 0.120 5 96937594 non coding transcript exon variant C/T snv 0.41 1
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs3764021
CLEC2D
1.000 0.120 12 9681032 splice region variant C/T snv 0.46 0.50 1
rs1326934
SORBS1
0.925 0.200 10 95524324 intron variant C/T snv 0.63 2
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
rs8007115 1.000 0.120 14 94871151 intergenic variant T/C snv 0.80 1
rs11160219 1.000 0.120 14 94869154 regulatory region variant A/G snv 0.75 1
rs11624318 1.000 0.120 14 94839675 intergenic variant C/A snv 0.15 1
rs754246590
SERPINA3
1.000 0.120 14 94614689 missense variant C/T snv 1.2E-05 7.0E-06 1
rs10255021
COL1A2
1.000 0.120 7 94402493 intron variant G/A snv 0.13 1
rs1460874866
SERPINA1
1.000 0.120 14 94382987 missense variant G/A snv 4.0E-06 1
rs597325
BACH2
0.925 0.160 6 90292775 intron variant A/G snv 0.69 2
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19