Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1060366
ATP1A1
1.000 0.040 1 116384040 synonymous variant A/G snv 1.3E-03 1.4E-03 2
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs161827
TNFRSF9
1.000 0.040 1 7921974 3 prime UTR variant T/C snv 0.12 2
rs199976415
NUDC ; NR0B2
1.000 0.040 1 26911982 missense variant G/A snv 6.0E-05 2.1E-05 2
rs35439639
AVPR1B
1.000 0.080 1 206109537 3 prime UTR variant C/G;T snv 2
rs35608965
AVPR1B
1.000 0.080 1 206116919 5 prime UTR variant A/G snv 4.9E-02 6.2E-02 2
rs3753886
TAF5L
1.000 0.040 1 229602423 synonymous variant T/A;G snv 5.2E-05; 0.56 2
rs59825600
LOC105376759 ; KAZN
1.000 0.040 1 14806568 intron variant G/A snv 0.11 2
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs952635
PDE4B
1.000 0.040 1 66226202 intron variant C/G;T snv 2
rs35810727
AVPR1B
1 206112629 intron variant G/A;T snv 1
rs750521766
LAD1
1 201389275 missense variant C/T snv 1.1E-04 3.5E-05 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21