Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs2300478
MEIS1
0.851 0.120 2 66554321 intron variant T/G snv 0.21 6
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs41305272
MAP2K5
0.851 0.120 15 67807105 3 prime UTR variant C/T snv 2.4E-02 6
rs113851554
MEIS1
0.882 0.080 2 66523432 intron variant G/A;T snv 5
rs1830084
SRPRB ; LOC105374116 ; TF
0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv 4
rs3810651
GABRQ ; LOC105373370
0.925 0.080 X 152652814 missense variant A/C;T snv 4
rs2280673
RAB6B
0.882 0.160 3 133839310 intron variant A/C;T snv 3
rs2412646
CLOCK ; TMEM165
0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs9296249
BTBD9
0.882 0.120 6 38398065 intron variant T/C snv 0.30 3
rs12469063
MEIS1
0.925 0.080 2 66537176 intron variant A/G snv 0.18 2
rs12593813
MAP2K5
1.000 0.080 15 67744514 intron variant A/G snv 0.53 2
rs179945
ATXN1
0.925 0.120 6 16396238 intron variant C/T snv 2
rs3104767
CASC16
0.925 0.080 16 52590826 intron variant G/T snv 0.49 2
rs4714156
BTBD9
0.925 0.120 6 38393336 intron variant C/T snv 0.36 2
rs693534
NOS1
1.000 0.080 12 117346913 intron variant G/A snv 0.36 2
rs7977109
NOS1
1.000 0.080 12 117292535 intron variant G/A;T snv 2
rs10208712 1.000 0.080 2 3986856 regulatory region variant A/G snv 0.26 1
rs1026732
MAP2K5
1.000 0.080 15 67802747 intron variant G/A snv 0.38 1
rs10952927
LOC107986816
1.000 0.080 7 88729746 intron variant A/G;T snv 1
rs111652004 1.000 0.080 15 47068169 intergenic variant G/T snv 8.6E-02 1