Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs9873580
IL12A-AS1
1.000 0.080 3 159911578 non coding transcript exon variant C/T snv 9.6E-02 1
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs971290 1.000 0.080 14 68805252 intergenic variant C/A;G;T snv 1
rs9491896
PTPRK
1.000 0.080 6 127979804 intron variant G/A snv 8.5E-02 1
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs9457515
C6orf99
1.000 0.080 6 158913093 intron variant T/C;G snv 1
rs9391227 1.000 0.080 6 104710759 regulatory region variant T/A snv 0.56 1
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 2
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs888208
NKX2-3
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25 3
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs859715 1.000 0.080 1 172790982 intron variant A/T snv 0.36 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs842647
REL
0.827 0.400 2 60892336 intron variant G/A snv 0.62 6
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs80209296
PTPN2
0.925 0.200 18 12860802 intron variant G/A snv 2