Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs10506481
MIR6502 ; IRAK3
0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs12048215
NLRP3
0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs1475145065
CTSG
0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs1764390
LOC105378642 ; GJA4 ; SMIM12
0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs352162 0.882 0.160 3 52218953 non coding transcript exon variant T/C snv 0.55 3
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs5743867
TOLLIP
0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs7119750
RELA
0.882 0.120 11 65655120 3 prime UTR variant C/G;T snv 3
rs773520745
IL12RB1
0.882 0.120 19 18075817 missense variant C/G;T snv 2.0E-05; 4.0E-06 3
rs773829498
SERPINE1
0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3
rs77874543
TNFRSF13C
0.882 0.080 22 41926712 missense variant G/C;T snv 6.1E-02 5.5E-02 3
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs41274221
MCM7 ; MIR106B ; MIR25 ; MIR93
0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs2069948
PROCR ; MMP24-AS1-EDEM2
0.851 0.160 20 35174686 non coding transcript exon variant C/T snv 0.55 0.62 5
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5