Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002922 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 1
rs10489276 1.000 0.040 1 172893799 intron variant C/T snv 0.31 1
rs10512734 1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29 1
rs10734105 1.000 0.040 10 131373856 intergenic variant G/A;C;T snv 1
rs10789230 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 1
rs10801047 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 1
rs10975003 0.882 0.080 9 5213687 intergenic variant T/C snv 0.43 1
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 1
rs1105267 1.000 0.040 13 20365097 intergenic variant G/A snv 0.54 1
rs1109863 1.000 0.040 16 50658453 intergenic variant G/A snv 0.69 1
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 1
rs11208994 1.000 0.040 1 67059360 regulatory region variant A/G;T snv 1
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 1
rs11229030 1.000 0.040 11 57435536 regulatory region variant C/T snv 0.55 1
rs11235667 0.925 0.120 11 73152652 intergenic variant A/G snv 2.3E-03 1
rs11265519 1.000 0.040 1 160909123 intergenic variant C/A snv 0.60 1
rs11616188 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 1
rs11894081 1.000 0.040 2 5523876 intergenic variant G/T snv 0.57 1
rs12035082 1.000 0.040 1 172929237 intron variant T/C snv 0.52 1
rs12552933 1.000 0.040 9 114759302 intergenic variant C/T snv 2.9E-02 1
rs12567232 1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27 1
rs12576495 1.000 0.040 11 93131841 upstream gene variant T/C snv 0.23 1
rs12663356 1.000 0.040 6 21430497 intergenic variant T/C snv 0.52 1
rs12922698 1.000 0.040 16 50815062 intergenic variant C/T snv 0.23 1
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 1