Source: GWASCAT ×
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 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17