Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4264325
TMEM179
1.000 0.120 14 104513149 intron variant T/C snv 0.97 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4392270 1.000 0.120 2 112921052 downstream gene variant A/G snv 0.93 1
rs2582532
PLD4
1.000 0.120 14 104926500 intron variant T/C snv 0.93 1
rs9267658
CYP21A2 ; SLC44A4 ; EHMT2-AS1
0.882 0.240 6 31878208 intron variant T/C snv 0.91 3
rs3132946
NOTCH4
0.882 0.240 6 32222251 intron variant A/G snv 0.91 3
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 4
rs800583 1.000 0.120 8 115852272 intergenic variant T/C snv 0.90 1
rs3130050
APOM ; BAG6
0.882 0.240 6 31650984 intron variant G/A snv 0.89 3
rs9267992 0.882 0.240 6 32252620 upstream gene variant G/A snv 0.89 3
rs325010
TMEM151B ; AARS2
1.000 0.120 6 44300181 3 prime UTR variant A/G snv 0.88 1
rs9267649 0.882 0.240 6 31857051 downstream gene variant A/G snv 0.88 3
rs757123
MSI1
1.000 0.120 12 120363020 intron variant A/G snv 0.89 0.88 1
rs4918037
SH3PXD2A
1.000 0.120 10 103653282 intron variant A/G snv 0.88 1
rs9268199
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32310858 intron variant G/A snv 0.87 1
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs7721046 1.000 0.120 5 63735364 intergenic variant T/C snv 0.86 1
rs2929973
CCN4
0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs1502644 1.000 0.120 5 3670892 intergenic variant C/A snv 0.85 2
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 4
rs6596147
FSTL4
1.000 0.120 5 133712084 intergenic variant T/A;C snv 0.84 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs1036199
HAVCR2
0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs7197
HLA-DRA
0.882 0.200 6 32444803 3 prime UTR variant T/C;G snv 0.83 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47