Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs11225055
ANGPTL5
1.000 0.120 11 101900702 intron variant T/A;C snv 1
rs6479891
JMJD1C
1.000 0.120 10 63246696 intron variant T/A;C snv 1
rs12416113
NRBF2
1.000 0.120 10 63136717 intron variant T/A snv 0.13 1
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs757278
CTTNBP2
1.000 0.120 7 117737591 intron variant G/T snv 0.44 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs12411988
REEP3
1.000 0.120 10 63555637 intron variant G/C snv 0.12 1
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs12652364 1.000 0.120 5 30835972 intergenic variant G/A;T snv 1
rs4746201
REEP3
1.000 0.120 10 63562621 intron variant G/A;T snv 2.2E-05; 0.16 1
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14