Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11021232 1.000 0.040 11 95587644 intron variant T/C snv 0.14 1
rs12201301 1.000 0.040 6 31039780 downstream gene variant G/A snv 2.7E-02 1
rs1264377 1.000 0.040 6 30797130 downstream gene variant G/A snv 0.13 1
rs13204672 1.000 0.040 6 32615019 intergenic variant A/G snv 0.12 1
rs1548514 1.000 0.040 6 30419691 downstream gene variant G/A;C;T snv 1
rs17188268 1.000 0.040 6 30231581 downstream gene variant G/A snv 3.2E-02 1
rs2248902 1.000 0.040 6 31266337 downstream gene variant G/A;T snv 1
rs3132649 1.000 0.040 6 30353280 downstream gene variant G/A snv 0.11 1
rs33986393 1.000 0.040 6 30456297 downstream gene variant A/G snv 0.16 1
rs34101875 1.000 0.040 6 30455581 non coding transcript exon variant G/A;C;T snv 1
rs35407515 1.000 0.040 6 30455446 non coding transcript exon variant A/G snv 0.17 1
rs4822024 1.000 0.040 22 41361643 downstream gene variant G/A;C snv 1
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 1
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 1
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 1
rs736374 0.925 0.080 11 35245397 regulatory region variant G/A snv 0.29 1
rs9261761 1.000 0.040 6 30405210 intergenic variant G/A snv 0.16 1
rs9261817 1.000 0.040 6 30410824 upstream gene variant A/C snv 0.16 1
rs9261821 1.000 0.040 6 30411297 upstream gene variant T/C snv 0.16 1
rs9261846 1.000 0.040 6 30414663 upstream gene variant G/C snv 0.17 1
rs9261919 1.000 0.040 6 30423946 downstream gene variant G/A snv 0.17 1
rs9261923 1.000 0.040 6 30424383 intergenic variant G/A snv 0.17 1
rs9261926 1.000 0.040 6 30424629 intergenic variant C/A;T snv 0.19 1
rs9261947 1.000 0.040 6 30426851 intergenic variant C/T snv 0.16 1
rs9271597 0.925 0.080 6 32623514 upstream gene variant T/A snv 0.39 1