Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10045403
ERAP1
0.882 0.040 5 96812030 upstream gene variant A/G snv 0.23 3
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 5
rs1013210 1.000 0.040 8 24259209 intergenic variant G/A;C;T snv 1
rs10280089 1.000 0.040 7 38667217 intergenic variant C/A;T snv 1
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1077667
TNFSF14
0.925 0.120 19 6668961 intron variant C/G;T snv 1
rs10781500
CARD9
1.000 0.040 9 136374886 upstream gene variant C/G;T snv 1
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs10870077
CARD9
0.827 0.120 9 136369439 intron variant C/G snv 0.38 5
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 2