Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6959212 7 38088724 intergenic variant T/C;G snv 3
rs10876432
SP7
12 53338107 intron variant G/A snv 2
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 2
rs4233949
LOC102724072
2 54432570 regulatory region variant C/A;G snv 2
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 2
rs4727338
SEM1 ; LOC105375411
7 96491363 intron variant G/C;T snv 2
rs4869742
CCDC170
6 151586613 intron variant C/A;G;T snv 2
rs6909279
CCDC170
6 151574321 intron variant G/C;T snv 2
rs7751941 6 151625523 downstream gene variant G/A;T snv 2
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 2
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 1
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 1
rs10505348
COLEC10
8 118960457 intergenic variant T/A;C snv 1
rs10808100
SEM1 ; LOC105375411
7 96501241 intron variant C/A;T snv 1
rs10872676 6 151622842 downstream gene variant C/A;T snv 1
rs1124674
ESR1
6 151759600 intron variant T/C;G snv 1
rs11573829
TNFRSF11B
8 118947384 intron variant T/A;C snv 1
rs11842146
LINC02341
13 42348370 intron variant C/G;T snv 1
rs11972702 7 38108059 regulatory region variant C/A;T snv 1
rs12197785 6 151639470 intergenic variant C/G;T snv 1
rs12197879
CCDC170
6 151574642 intron variant C/G;T snv 1
rs12742784 1.000 0.080 1 22355873 intergenic variant C/A;T snv 1
rs12861586 13 42336328 upstream gene variant C/A;T snv 1
rs13204965 6 126845927 intron variant A/C;T snv 1
rs1324003
LINC02341
13 42401990 intron variant C/G;T snv 1