Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 1
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 1
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 1
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 1
rs11199914 0.925 0.080 10 121334387 intergenic variant C/T snv 0.40 1
rs11242675 0.925 0.080 6 1318643 downstream gene variant C/T snv 0.58 1
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 1
rs11820646 0.925 0.080 11 129591276 upstream gene variant T/C;G snv 1
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 1
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 1
rs204247 0.925 0.080 6 13722291 intergenic variant G/A snv 0.59 1
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 1
rs2494251 0.925 0.080 1 159311361 downstream gene variant G/A;C snv 1
rs2823093 0.882 0.080 21 15148511 intergenic variant G/A snv 0.32 1
rs3903072 0.925 0.080 11 65815595 intergenic variant G/T snv 0.37 1
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 1
rs554219 0.925 0.080 11 69516874 regulatory region variant C/A;G;T snv 1
rs614367 0.882 0.080 11 69513996 intergenic variant C/T snv 0.14 1
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 1
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 1
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 1
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 1
rs9693444 0.925 0.080 8 29652100 intergenic variant A/C snv 0.66 1
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 1