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
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs765797019
PIK3CD
1 9720754 missense variant C/T snv 3.3E-05 3.5E-05 1
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4744411
LOC101928119 ; AOPEP
0.925 0.040 9 94926763 intron variant G/A;C;T snv 3
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs7538427
GTF2B
1.000 0.080 1 88873739 intron variant C/T snv 0.93 2
rs305217
PKN2
1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs761234173
CDH13
1.000 0.040 16 83783345 missense variant G/A snv 4.0E-06 2
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs3827440
GPR174 ; LOC107985690
0.851 0.120 X 79171491 missense variant T/A;C snv 5.5E-06; 0.51 6
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13