Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs1475539937
TLR9
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06 5
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs12992492 1.000 0.040 2 203836831 intergenic variant A/G snv 0.40 2
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 2
rs2893008
IL21-AS1
4 122631659 intron variant A/G snv 5.1E-02 2
rs6706689
PUS10
2 60943910 intron variant A/G snv 0.48 2
rs6517774 21 17449955 non coding transcript exon variant A/G snv 0.34 1
rs8176928
TRAP1 ; DNASE1
16 3656184 missense variant A/G snv 1.0E-03 4.0E-03 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs12115114 1.000 0.080 8 63477322 non coding transcript exon variant A/G;T snv 2