Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11164654 1 92502755 regulatory region variant T/C snv 0.85 2
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 3
rs11218721 11 122634009 regulatory region variant C/A snv 0.37 1
rs11220462
ST3GAL4
11 126374057 intron variant G/A snv 0.12 2
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs112374545
SMARCA4
19 11078223 intron variant C/T snv 0.11 2
rs112595563
DDX28 ; DUS2
16 68020885 intron variant A/G snv 0.21 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs112959129
ABHD11-AS1
7 73733661 upstream gene variant -/CA delins 1
rs113190300 19 11080015 downstream gene variant C/A;G;T snv 2
rs113759232
LINC02499
4 73522447 intron variant G/T snv 3.9E-03 2
rs113932726
ZPR1
11 116779922 intron variant C/T snv 9.8E-03 1
rs11406672
KPNA1
3 122507441 intron variant AA/-;A;AAA;AAAA;AAAAA;AAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA delins 1
rs114067101 6 32490183 intergenic variant A/G snv 6.1E-05 2
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs114197570 19 11085594 upstream gene variant C/T snv 3.3E-03 2
rs11456863 3 12230419 regulatory region variant T/-;TT;TTT;TTTTTTTTTTT delins 3
rs114846969 19 11080521 downstream gene variant G/A snv 0.12 1
rs11485618
DOCK7
1 62628536 3 prime UTR variant A/G snv 0.34 1
rs115485095
CYP21A2 ; EHMT2
6 31888293 intron variant G/A snv 3