Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35201538 1.000 0.040 9 33422490 intergenic variant -/T;TT delins 1
rs11375254
TP63
0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 1
rs7182948
FAM227B ; LOC105370811
1.000 0.040 15 49549483 intron variant A/C;G;T snv 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 1
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 6
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 3
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 3
rs62560775
CDKN2B-AS1
0.925 0.080 9 22052069 intron variant A/G snv 0.13 2
rs11632038
GALK2
1.000 0.040 15 49314101 intron variant A/G snv 0.15 1
rs17038564
ACTR2
1.000 0.040 2 65268924 3 prime UTR variant A/G snv 5.3E-02 1
rs184697115 1.000 0.040 5 16005668 intergenic variant A/G snv 6.3E-03 1
rs2316515
IRF4
1.000 0.040 6 410848 3 prime UTR variant A/G snv 0.52 1
rs2495239
FOXP4-AS1
1.000 0.040 6 41522750 intron variant A/G snv 0.84 1
rs28516445 1.000 0.040 15 49667937 intergenic variant A/G snv 0.18 1
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 1