Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7323466 13 100019615 intergenic variant T/C snv 0.64 1
rs2503099
LOC105377911
6 100162225 regulatory region variant A/G snv 0.18 1
rs2073267 6 100167776 TF binding site variant A/G snv 0.22 1
rs4851284
LONRF2
2 100278425 3 prime UTR variant C/T snv 0.67 1
rs2151131
TEX10
9 100346659 intron variant C/G snv 0.84 0.85 1
rs7122422
SBF2
11 10045715 intron variant G/C snv 0.37 1
rs10840349
SBF2
11 10054883 intron variant A/G;T snv 1
rs6747755
NPAS2
2 100961996 intron variant G/A snv 0.30 1
rs9557704
ITGBL1
13 101575144 intron variant A/G;T snv 1
rs421168
CUX1
7 102050604 intron variant G/A snv 0.53 1
rs372321
CUX1
7 102077726 intron variant G/A snv 0.17 1
rs367026
CUX1
7 102085358 intron variant T/C snv 0.49 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs140572498
LOC105369944
12 102569167 intergenic variant C/T snv 0.12 1
rs28408682
TRIM8
10 102643553 5 prime UTR variant A/G snv 0.67 1
rs12590238
TRAF3
14 102883860 intron variant C/G snv 0.24 1
rs2061708
COL11A1
1 102951647 intron variant G/A;C;T snv 2
rs17154889
PAM
5 102969361 intron variant C/A snv 0.27 1
rs2061705
COL11A1
1 102976258 intron variant A/G;T snv 1
rs12419064 11 10299061 upstream gene variant A/G snv 0.44 1
rs1415364
COL11A1
1 103087259 intron variant C/T snv 0.48 1
rs2513987 11 103106542 upstream gene variant G/A;C snv 1
rs2957658
AMPD3 ; CAND1.11
11 10371921 intron variant G/A snv 0.45 1
rs2161097 5 104609477 intron variant C/T snv 0.40 1
rs11042841
AMPD3
11 10483662 intron variant C/G snv 0.70 1