Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1936797 6 127111512 intron variant A/G snv 0.33 3
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 3
rs2287921
RASIP1
1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 3
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs340025
RORA ; RORA-AS1
15 60616108 intron variant T/A;C snv 3
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs643434
ABO
9 133266942 intron variant A/G;T snv 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 3
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 2
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2