Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs52820871 0.827 0.160 18 60371599 missense variant T/G snv 6.9E-03 7.6E-03 6
rs1042571 0.882 0.120 2 25161018 3 prime UTR variant G/A snv 0.16 3