Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 7
rs10194635
LINC01104
0.807 0.120 2 100217755 intron variant T/A;G snv 6
rs10213692
ANKRD55
0.807 0.120 5 56146422 intron variant T/C snv 0.17 6
rs10849448
LTBR
0.807 0.120 12 6384185 5 prime UTR variant A/G snv 0.82 6
rs11074967
LOC105371082 ; LOC400499 ; RMI2
0.807 0.120 16 11377557 intron variant C/G snv 0.36 6
rs11714843
TIMMDC1
0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
rs1479924 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 6
rs149850873
PTPN2
0.807 0.120 18 12885121 intron variant G/A snv 1.7E-02 6
rs27293
LNPEP
0.807 0.120 5 97021474 intron variant A/G;T snv 6
rs2847293 0.807 0.120 18 12782449 downstream gene variant A/G;T snv 6
rs34132030
LINC02341
0.807 0.120 13 42481900 intron variant C/T snv 0.26 6
rs3825568
ZFP36L1
0.807 0.120 14 68793871 5 prime UTR variant C/G;T snv 6
rs45539732
STAT1
0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 6
rs4648881 0.807 0.120 1 24870664 intergenic variant G/A snv 0.47 6
rs6946509 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 6
rs7069750
FAS
0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 6
rs7127214
PRR5L
0.807 0.120 11 36322143 intron variant C/G;T snv 6
rs72698115
IL6R ; IL6R-AS1
0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6
rs73300638
JAZF1
0.807 0.120 7 28147725 intron variant A/C;G snv 6
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 6
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs114940806
KLF17
0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs1178121
HDAC9
0.882 0.120 7 18723029 intron variant C/A snv 0.31 3
rs12517545
LINC01331
0.882 0.120 5 74384489 intron variant G/A snv 0.13 3