Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 1
rs10454134 1.000 0.200 2 48420887 TF binding site variant G/A snv 0.14 1
rs116799036 1.000 0.200 6 31381371 downstream gene variant G/A snv 1
rs11769828 1.000 0.200 7 150534221 intergenic variant C/T snv 0.19 1
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 1
rs12141431 1.000 0.200 1 67281340 downstream gene variant G/C snv 0.23 1
rs224127 1.000 0.200 10 62701513 intron variant A/G snv 0.69 1
rs2848713 1.000 0.200 6 31416702 intron variant G/A snv 5.3E-02 1
rs6845297 1.000 0.200 4 74393688 downstream gene variant G/A snv 0.48 1
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 1
rs855873
AIM2
1.000 0.200 1 159077922 intron variant A/G snv 0.84 1
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 1
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38 1
rs408290
C3
1.000 0.200 19 6702011 intron variant G/C;T snv 1
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62 1
rs1970000
CD274
1.000 0.200 9 5465036 intron variant C/A;G snv 1
rs7028891
DELEC1
0.925 0.280 9 114882735 intron variant A/G snv 0.50 1
rs4073153
DNLZ ; CARD9
1.000 0.200 9 136364897 non coding transcript exon variant A/G snv 0.40 1
rs13154629
ERAP1
1.000 0.200 5 96786754 non coding transcript exon variant C/T snv 0.16 1
rs1065407
ERAP1 ; CAST ; LOC102724748
1.000 0.200 5 96776379 3 prime UTR variant T/A;G snv 3.3E-05; 0.26 1
rs943899383
F5
1.000 0.200 1 169586343 frameshift variant C/- delins 1
rs9577873
GAS6 ; GAS6-AS1
1.000 0.200 13 113825282 intron variant G/A;T snv 1
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 1
rs9260997
HLA-A
1.000 0.200 6 29995539 upstream gene variant T/C snv 0.90 1
rs6940
IFI16
1.000 0.200 1 159054878 missense variant A/T snv 0.15 0.17 1