Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;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
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs12339348
LOC107987046 ; IL33
1.000 0.080 9 6233082 intron variant A/G;T snv 2
rs1241357 1.000 0.080 8 56793197 intergenic variant G/A snv 2
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv 2
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 2
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 2