Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4073285
MMEL1
0.925 0.200 1 2608357 intron variant C/T snv 0.40 2
rs6696533 0.925 0.200 1 198764438 intergenic variant T/C snv 0.28 2
rs10800746
INAVA
1.000 0.080 1 200912264 intron variant C/T snv 0.32 1
rs12142280 1.000 0.080 1 172895512 intron variant T/A snv 0.21 1
rs12727642 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 1
rs2157453 1.000 0.080 1 172894808 intron variant G/A snv 0.31 1
rs4445406
MMEL1
1.000 0.080 1 2607961 intron variant T/C snv 0.41 1
rs59655222
INAVA
1.000 0.080 1 200906769 intron variant T/C snv 0.22 1
rs6691768
NFIA
1.000 0.080 1 61326191 intron variant G/A;C snv 1
rs859715 1.000 0.080 1 172790982 intron variant A/T snv 0.36 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs842647
REL
0.827 0.400 2 60892336 intron variant G/A snv 0.62 6
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 4
rs771541567
APOB
0.851 0.120 2 21029900 missense variant G/A;T snv 8.0E-06; 2.0E-05 4