Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 1
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 1
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12714414 2 651407 intergenic variant T/C snv 0.18 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs1320336 2 650012 intergenic variant G/A snv 0.18 2
rs1320337 2 649867 intergenic variant A/T snv 0.19 2
rs1320338 2 649347 intergenic variant T/G snv 0.18 2
rs13386517 2 650479 regulatory region variant G/A;C snv 2
rs13386627 2 650560 regulatory region variant G/C;T snv 2
rs13386964 2 650828 regulatory region variant G/A snv 0.18 2
rs13388043 2 637597 regulatory region variant C/A;T snv 2
rs13393304 2 637830 regulatory region variant A/C;G snv 2
rs13396935 2 653195 intergenic variant G/A snv 0.18 2