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
rs888208
NKX2-3
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25 3
rs11190141
LINC01475 ; NKX2-3
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40 3
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 3
rs11596008
LINC01475
0.925 0.040 10 99527557 intron variant C/T snv 0.29 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 3
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs71485777 1.000 0.040 10 99523571 upstream gene variant CCC/GCA mnv 1
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs9554587 0.827 0.120 13 99388400 downstream gene variant A/G snv 0.17 5
rs3742130
GPR18 ; UBAC2
0.925 0.040 13 99255087 synonymous variant G/A snv 0.16 0.16 3
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs746482334
ANKS1B ; APAF1
1.000 0.040 12 98732507 missense variant A/G snv 4.0E-06 1
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22 4
rs1476273292
APAF1
1.000 0.040 12 98712328 missense variant G/A snv 4.0E-06 1
rs13420683
ZAP70
1.000 0.040 2 97719889 intron variant C/A;T snv 1
rs1363907
ERAP2 ; ERAP1
1.000 0.040 5 96917099 intron variant G/A snv 0.38 2
rs2910686
ERAP2 ; ERAP1
0.827 0.120 5 96916885 intron variant T/C snv 0.42 5
rs1437138510
ERAP2 ; ERAP1
1.000 0.040 5 96909646 missense variant T/C snv 4.0E-06 1
rs2549794
ERAP2 ; ERAP1
1.000 0.040 5 96908845 intron variant C/T snv 0.62 1
rs2248374
ERAP1 ; ERAP2
0.851 0.120 5 96900192 splice region variant A/G snv 0.55 0.54 4
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs2549803
ERAP1
0.827 0.120 5 96839226 intron variant C/T snv 0.27 5
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14