Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs5743611
TLR1
0.807 0.160 4 38798593 missense variant C/G snv 6.9E-02 7.1E-02 7
rs1545620
MYO9B
0.827 0.080 19 17192965 missense variant T/A;G snv 1.3E-05; 0.52 6
rs1466065840
NOD2
1.000 0.040 16 50712168 frameshift variant C/- del 1
rs749720540
NOD2
1.000 0.040 16 50712168 missense variant C/A;G;T snv 4.0E-06; 5.6E-05 1