Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs2278986
SCARB1
0.925 0.120 12 124814823 intron variant A/G snv 0.28 2
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs7042521
CACNA1B ; LOC100133077
1.000 0.120 9 137889440 intron variant C/G snv 0.31 1
rs11137351
CACNA1B ; LOC101928786
1.000 0.120 9 138045676 intron variant C/G snv 0.23 1
rs10780199
CACNA1B
1.000 0.120 9 138058845 intron variant G/A snv 0.36 1
rs774320676
CTSS
1.000 0.120 1 150750091 missense variant A/T snv 4.0E-06 1
rs2275235
CTSS
1.000 0.120 1 150757803 intron variant A/G snv 0.34 1
rs928508030
CTSS
1.000 0.120 1 150765698 splice region variant G/A snv 1
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1044009
NOTCH3
1.000 0.120 19 15160960 missense variant G/A snv 0.71 0.69 1
rs1044006
NOTCH3
1.000 0.120 19 15174241 synonymous variant T/A;C snv 0.86 1
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17