Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2238631
TBXA2R
1.000 0.080 19 3604301 intron variant T/C snv 0.84 1
rs8089787
MIR133A1HG ; MIB1 ; MIR133A1
1.000 0.080 18 21826640 non coding transcript exon variant T/C snv 0.84 1
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 2
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs801429
FBXL20
1.000 0.080 17 39279125 intron variant T/C snv 0.81 1
rs413382 1.000 0.080 9 6142948 intergenic variant C/A snv 0.81 2
rs3751972
LYRM9
1.000 0.080 17 27879388 3 prime UTR variant C/A snv 0.80 1
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs4436440 1.000 0.080 1 202082885 TF binding site variant T/A snv 0.80 1
rs188074962 0.925 0.080 12 120927628 intergenic variant G/A snv 0.79 2
rs1538084 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 1
rs2353275
GRID1
1.000 0.080 10 86305355 intron variant T/C snv 0.79 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1454197
MYH15
1.000 0.080 3 108519798 intron variant G/T snv 0.79 1
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs6587688 1.000 0.080 1 152557146 intergenic variant T/C snv 0.78 1
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs6736411
WDPCP
0.925 0.120 2 63446926 intron variant G/A snv 0.78 2
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs10800812 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52