Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs12752888
LINC02784
0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs1557372 1.000 0.040 21 41460614 downstream gene variant C/T snv 0.40 2
rs117070989 1.000 0.040 6 137490510 downstream gene variant C/A snv 8.3E-03 1
rs12468965 1.000 0.040 2 53528621 downstream gene variant G/A snv 1.8E-02 1
rs146594485 1.000 0.040 20 3776090 downstream gene variant G/A snv 6.1E-03 1
rs149028778
LOC105371775 ; KRT24
1.000 0.040 17 40695009 downstream gene variant C/T snv 9.7E-03 1
rs150616616 1.000 0.040 5 121366663 downstream gene variant C/G;T snv 1
rs150759334 1.000 0.040 4 60800528 downstream gene variant T/C snv 9.4E-03 1
rs79947075 1.000 0.040 17 40764791 downstream gene variant C/T snv 9.5E-03 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs2731880 0.925 0.040 5 36603282 upstream gene variant T/C snv 0.52 3
rs7759295
LOC105375056
1.000 0.040 6 41168112 upstream gene variant C/G;T snv 2
rs113793030 1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02 1