Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 3
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52 2
rs10760706
STX17
1.000 0.040 9 99961410 intron variant C/T snv 0.69 1
rs12183587
RAET1M
1.000 0.040 6 150033472 non coding transcript exon variant T/C;G snv 1
rs1431704
MIR924HG
1.000 0.040 18 39273770 intron variant T/C snv 7.0E-02 1
rs17031716
MAGI3
1.000 0.040 1 113609225 intron variant C/A snv 0.18 1
rs17479692
SLC16A12
1.000 0.040 10 89528702 intron variant T/G snv 9.3E-02 1
rs2216164
IFNG-AS1
1.000 0.040 12 68140560 intron variant A/G snv 0.49 1
rs247459
VDAC1
1.000 0.040 5 134046765 intergenic variant T/A;C snv 1
rs2666138 1.000 0.040 2 36104014 intergenic variant G/A;T snv 1
rs2847266 1.000 0.040 18 12773339 intron variant C/T snv 0.69 1
rs3099624 1.000 0.040 1 11436937 intergenic variant C/T snv 0.34 1
rs3789129
ACOXL
1.000 0.040 2 110940463 intron variant A/C snv 0.18 1
rs3862469
CLEC16A
1.000 0.040 16 11100223 intron variant C/T snv 0.35 1
rs4738296
KCNB2
1.000 0.040 8 72945304 upstream gene variant A/C snv 7.9E-02 1
rs4916209 1.000 0.040 1 173164350 intergenic variant G/A snv 0.33 1
rs574087
LOC102723878
1.000 0.040 11 64335476 upstream gene variant A/G snv 0.28 1
rs6906608
IRF4
1.000 0.040 6 411554 downstream gene variant C/A snv 0.11 1
rs7099812
MALRD1
1.000 0.040 10 19689469 intron variant T/G snv 0.41 1
rs7228576
LINC01254 ; LOC105371988
1.000 0.040 18 10408495 intron variant C/T snv 0.19 1
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs7682481 1.000 0.040 4 122602871 regulatory region variant G/A;C snv 1
rs9479482 1.000 0.040 6 150036876 downstream gene variant T/C snv 0.36 1
rs9982439 1.000 0.040 21 42329090 regulatory region variant T/C snv 3.1E-02 1
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 2