Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs148314165 0.925 0.160 6 137908902 intergenic variant T/- delins 2.0E-02 3
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs4845384
ADAR
1.000 0.080 1 154615193 intron variant A/G snv 0.69 1
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs76844316
BTLA
1.000 0.080 3 112469762 missense variant T/G snv 2.4E-02 2.2E-02 1
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs78900671
COL22A1
1.000 0.080 8 138653967 intron variant G/A;C snv 1
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 5
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22