Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2928442
LOC105378313
1.000 0.080 10 57386706 intergenic variant T/A;C snv 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2853209
ADAM33
0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs5875060
SCGN
1.000 0.080 6 25701740 3 prime UTR variant T/-;TT;TTT delins 2
rs137939366
ELSPBP1
1.000 0.080 19 48019433 intron variant T/- del 1.5E-02 2
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs10836538
PRR5L
0.925 0.080 11 36343703 intron variant G/T snv 0.30 2
rs2052690
MRVI1
0.925 0.080 11 10642486 intron variant G/T snv 0.22 2
rs3116989
LOC105375021 ; HLA-DPA3
0.925 0.080 6 33131761 intron variant G/T snv 0.16 2
rs35570272
GLB1
0.925 0.080 3 33006170 intron variant G/T snv 0.36 2
rs3902025
GSDMA
0.925 0.080 17 39963001 intron variant G/T snv 0.56 2
rs17033506 1.000 0.080 3 35598334 intergenic variant G/T snv 2.8E-02 1
rs2037986
LINC01697
1.000 0.080 21 28104158 intron variant G/T snv 0.44 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs73985228
ORMDL3
0.882 0.080 17 39922412 3 prime UTR variant G/C;T snv 3
rs340934 0.925 0.080 9 6081804 intergenic variant G/C;T snv 2
rs44707
ADAM33
0.925 0.080 20 3670579 non coding transcript exon variant G/C;T snv 2
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs16917204
BDNF-AS
0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs142161979
ANKS1B
1.000 0.080 12 99392036 intron variant G/C snv 3.5E-03 2