Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10129035 12 83706429 intergenic variant T/A;C snv 1
rs1016680 17 37514283 downstream gene variant A/C snv 0.74 1
rs1023667 5 158541893 intron variant G/A;C snv 1
rs10252662 7 44771624 downstream gene variant C/T snv 0.37 1
rs1037117 15 101528455 upstream gene variant G/A snv 0.28 1
rs10772108 12 9746454 intergenic variant C/G;T snv 1
rs10797857 1 183175588 intergenic variant C/A;G snv 1
rs10808536 8 86156820 upstream gene variant G/A snv 0.26 1
rs1082428 6 137886592 downstream gene variant C/G;T snv 1
rs10858963 12 90152611 intergenic variant T/A;C snv 1
rs10883756 10 102640355 upstream gene variant T/A;C snv 1
rs10889574 1 65683658 intergenic variant G/A snv 0.34 1
rs10935478 3 98709311 non coding transcript exon variant C/T snv 0.37 1
rs10961195 9 13676534 intron variant T/C snv 0.50 1
rs10973700 9 38196120 regulatory region variant G/C snv 0.49 1
rs1098099 10 74731289 intergenic variant C/T snv 0.81 1
rs10986338 9 124428953 regulatory region variant G/A snv 0.53 1
rs11164861 1 93012974 downstream gene variant C/T snv 0.22 1
rs11169751 12 51186388 downstream gene variant A/G snv 0.16 1
rs11231675 11 55954235 downstream gene variant A/T snv 0.50 1
rs11264422 1 155938032 upstream gene variant T/A snv 0.48 1
rs113028115 19 42263441 intergenic variant T/C snv 0.10 1
rs113164910 6 32459228 downstream gene variant A/C snv 1
rs113418195 6 31253748 intergenic variant C/G snv 1
rs113799399 3 141207949 intergenic variant C/T snv 0.22 1