Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003878
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs10484566
PSMB9
0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs1077393
BAG6
0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs1214611
CD247
0.925 0.200 1 167479867 intron variant A/G snv 0.54 2
rs12177980
LOC102725019
0.925 0.200 6 32718307 non coding transcript exon variant G/A snv 0.37 2
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs12660382
HCP5
0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs147846074
AIRE
0.925 0.200 21 44289743 missense variant C/G;T snv 1.2E-05; 3.2E-05; 4.0E-06 3
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs2027856 0.925 0.200 6 32434928 upstream gene variant G/A snv 0.18 2
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs2050189
TSBP1 ; TSBP1-AS1
0.925 0.200 6 32371870 5 prime UTR variant T/C;G snv 0.18 2
rs206015
NOTCH4
0.925 0.200 6 32214982 intron variant G/A snv 0.15 2
rs2064478
COL11A2P1
0.925 0.200 6 33104489 intron variant C/T snv 0.28 2
rs2071540
TAP1 ; PSMB9 ; PSMB8-AS1 ; PSMB8
0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 2
rs2071554
HLA-DOB
0.925 0.200 6 32816899 missense variant C/A;T snv 4.1E-06; 6.2E-02 2
rs2076537
TSBP1 ; TSBP1-AS1
0.925 0.200 6 32349858 non coding transcript exon variant G/A snv 0.37 0.42 2
rs2156875
HLA-B
0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs2244839
HCP5 ; HCG26
0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs2256965
LST1
0.925 0.200 6 31587353 non coding transcript exon variant A/G;T snv 0.60 2
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 7
rs2267644
NOTCH4
0.925 0.200 6 32224783 upstream gene variant G/A snv 4.9E-02 2