Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999556 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 2
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs9987128
CSMD1
1.000 0.040 8 3122601 intron variant A/G snv 0.17 1
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs984473166
SSTR4
1.000 0.040 20 23035661 missense variant G/T snv 1
rs982610810
TNF
1.000 0.040 6 31575766 missense variant G/A snv 4.2E-06 1
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9807841
QTRT1
1.000 0.040 19 10706980 intron variant T/C snv 0.73 1
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19 5
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 6
rs963986
CAVIN1
1.000 0.040 17 42409561 intron variant G/C snv 0.15 1
rs9554587 0.827 0.120 13 99388400 downstream gene variant A/G snv 0.17 5
rs955155 1.000 0.040 19 39238839 upstream gene variant G/A snv 0.20 1
rs953861
LOC285626
1.000 0.040 5 159345574 intron variant G/A;C snv 1
rs9533962 1.000 0.040 13 44760058 regulatory region variant C/T snv 0.47 1
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9513593
GPR183 ; UBAC2
1.000 0.040 13 99298006 intron variant G/A snv 0.71 1
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs9494840 0.827 0.120 6 137641937 regulatory region variant T/A snv 4.3E-05 5
rs9491891 0.827 0.120 6 127956006 intergenic variant A/G snv 0.12 5
rs9487605
MFSD4B
1.000 0.040 6 111261682 intron variant A/C;G;T snv 1
rs9481169 1.000 0.040 6 111608659 upstream gene variant G/T snv 0.17 1