Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72938315
CYP20A1
2 203256340 intron variant C/G snv 0.11 1
rs10975277
ERMP1 ; RIC1
9 5774661 3 prime UTR variant G/A;C snv 1
rs57347370
GJA1
6 121440942 intron variant G/T snv 0.25 1
rs9828592
GLB1
3 33002847 intron variant T/C snv 0.49 1
rs117552144
GNA15
19 3136093 5 prime UTR variant C/T snv 3.8E-02 1
rs9303279
GSDMB
17 39917715 non coding transcript exon variant G/A;C snv 1
rs12722547
IL2RA
10 6030130 intron variant G/C snv 7.8E-03 1
rs11567694
IL7R ; LOC105374724
5 35857602 intron variant A/G snv 0.25 1
rs67872952
IQCH
15 67269260 intron variant C/T snv 0.22 1
rs111782388
ITK
5 157202838 intron variant C/T snv 6.3E-02 1
rs1779774
LGSN
6 63500578 intergenic variant C/G;T snv 1
rs10965935
LOC101929563
9 23581213 intron variant C/G;T snv 0.38 1
rs7134784
PLXNC1
12 94188701 intron variant T/C snv 0.83 1
rs75567729
PTPRC
1 198641406 intron variant A/G snv 8.4E-02 1
rs8126516
RUNX1
21 35080321 intron variant G/A snv 0.13 1
rs30526
SEPTIN8
5 132774274 intron variant T/A;C snv 1
rs76848919
SOCS3
17 78356473 upstream gene variant G/A;C snv 1
rs41283642
TGFBR1
9 99153605 3 prime UTR variant C/G;T snv 1
rs10788639
TSPAN14
10 80473469 intron variant C/G snv 0.64 1
rs11178649
TSPAN8
12 71139458 intron variant G/T snv 0.32 1
rs12889006
ZFP36L1
14 68793846 5 prime UTR variant G/A;C snv 1
rs35621564 1.000 0.080 7 20547220 regulatory region variant A/C;G snv 2
rs72833417 1.000 0.080 17 47795683 intergenic variant A/T snv 9.7E-02 2
rs75130836 11 76180138 intergenic variant T/C snv 1.2E-02 2
rs8020739 14 35413286 TF binding site variant G/T snv 0.67 2