Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 19
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 17
rs11571818 0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 17
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs115392158 0.708 0.280 6 31347004 intron variant A/G snv 17
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs11119608 0.708 0.280 1 210816167 intron variant T/G snv 0.21 17