Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs12023876
ADORA1
0.925 0.080 1 203124073 intron variant G/A;T snv 2
rs12531500 0.925 0.080 7 20504586 intergenic variant A/C;G snv 2
rs13090972 1.000 0.080 3 89027746 intergenic variant C/G;T snv 2
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs142320277
LRP1B
1.000 0.080 2 140665410 intron variant G/A;C snv 2
rs17103286 0.925 0.080 14 35415835 regulatory region variant A/C;G snv 2
rs1861245
IL18R1 ; IL1RL1
0.925 0.080 2 102350446 intron variant C/T snv 2
rs1893380 0.925 0.080 18 51121270 intergenic variant G/A;C;T snv 2
rs2299012
RAD50
0.925 0.080 5 132581248 intron variant A/C;T snv 2