Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 7
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 7
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs1051794
MICA
0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 5
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21 5
rs2259571
AIF1
0.925 0.120 6 31616050 5 prime UTR variant T/G snv 0.28 5
rs2428486 0.925 0.120 6 31386327 upstream gene variant T/C snv 0.42 5
rs2523467
MICA-AS1
0.925 0.120 6 31395153 non coding transcript exon variant C/A;T snv 0.40 5
rs2523619
HLA-B
0.925 0.120 6 31350367 intron variant T/C snv 0.23 5
rs2523674
HCP5
0.925 0.120 6 31469012 non coding transcript exon variant A/G snv 0.54 5
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34 5
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29 5
rs2844477 0.925 0.120 6 31610995 upstream gene variant T/A;C snv 0.29 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs2844795
TRIM31 ; TRIM31-AS1
0.925 0.120 6 30106070 intron variant C/G;T snv 5
rs2857697
AIF1
0.925 0.120 6 31617442 upstream gene variant C/T snv 0.34 5
rs3130983
PSORS1C1 ; CDSN
0.925 0.120 6 31117015 synonymous variant C/T snv 0.57 0.58 5
rs3871466
MUC22
0.925 0.120 6 31015906 intron variant T/C snv 0.12 5
rs3873379
LINC02571 ; HLA-B
0.925 0.120 6 31294392 intron variant T/C snv 0.35 5
rs4394275
HLA-B
0.925 0.120 6 31350400 intron variant G/A snv 0.27 5
rs4713380
LINC00243
0.925 0.120 6 30817496 intron variant T/C snv 0.17 5
rs4713385
LINC00243
0.925 0.120 6 30819816 intron variant G/A snv 0.17 5