Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 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
rs12141431 1.000 0.200 1 67281340 downstream gene variant G/C snv 0.23 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs224127 1.000 0.200 10 62701513 intron variant A/G snv 0.69 1
rs2517411 1.000 0.200 6 30992490 downstream gene variant T/C;G snv 1
rs2848479 1.000 0.200 11 98216871 intergenic variant C/T snv 0.40 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
rs6910516 1.000 0.200 6 31376050 non coding transcript exon variant A/C;G snv 1
rs9266406 1.000 0.200 6 31368641 intron variant G/A snv 0.22 1
rs9266490 1.000 0.200 6 31372381 intron variant A/G snv 0.22 1
rs9380217 1.000 0.200 6 31083776 downstream gene variant C/T snv 6.4E-02 1
rs146597836
ADA2
1.000 0.200 22 17189987 missense variant C/T snv 1.8E-03 1.6E-03 1
rs750868279
ADA2
1.000 0.200 22 17203576 missense variant G/A snv 5.2E-05 4.9E-05 1
rs855873
AIM2
1.000 0.200 1 159077922 intron variant A/G snv 0.84 1
rs408290
C3
1.000 0.200 19 6702011 intron variant G/C;T snv 1
rs2073716
CCHCR1
1.000 0.200 6 31155220 intron variant C/G snv 6.8E-02 1
rs1970000
CD274
1.000 0.200 9 5465036 intron variant C/A;G snv 1
rs386579334
CDSN ; PSORS1C1
1.000 0.200 6 31119356 intron variant C/T snv 1