Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs367814475
IVD
0.925 0.080 15 40415482 missense variant G/C;T snv 8.0E-06; 4.0E-06 9
rs121908261
INS-IGF2 ; INS
0.851 0.120 11 2160809 missense variant G/A snv 5
rs745343884
BTD
0.882 0.120 3 15644335 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs587777042
CYC1
0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs2251101
IDE
0.882 0.160 10 92451547 downstream gene variant C/A;T snv 3
rs7214136
SREBF1
0.882 0.120 17 17816675 missense variant C/T snv 6.4E-03 1.9E-02 3
rs758604661
ABCC8
0.925 0.120 11 17474898 missense variant A/G snv 8.0E-06 2
rs1014048269
OXCT1
1.000 0.040 5 41805681 missense variant G/A;C snv 4.0E-06 1